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Genes Associated with Diseases

10,706 "disease genes" are currently present in the GeneCards database

Showing 452 "disease genes" starting with 'G'

1  3  5  A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z  Complete list

The genes listed here cause, predispose or protect from diseases

GeneCards Gene Gene Name Locus MalaCards Disorders (sorted by relevance)
G0S2 G0/G1switch 2 1q32.2 Van Der Woude Syndrome
G3BP2 GTPase activating protein (SH3 domain) binding protein 2 4q21.1 Nodular Malignant Melanoma
G6PC glucose-6-phosphatase, catalytic subunit 17q21.31 Glycogen Storage Disease Type 1A,  Glycogen Storage Disease,  Glycogen Storage Disease Type 1B,  Tendinitis,  Ocular Hypertension,  Juvenile Hereditary Hemochromatosis,  Favism,  Hepatocellular Adenoma,  Glycogen Storage Disease I,  Hyperuricemia,  Sudden Infant Death Syndrome,  Hypoglycemia,  Galactosemia,  Portal Hypertension Insulin Resistance Show all 15
G6PC2 glucose-6-phosphatase, catalytic, 2 2q31.1 Type 1 Diabetes Mellitus
G6PC3 glucose 6 phosphatase, catalytic, 3 17q21.31 Dursun Syndrome,  Severe Congenital Neutropenia, Autosomal Recessive, 4,  Severe Congenital Neutropenia,  Neutropenia Myotonia Show all 5
G6PD glucose-6-phosphate dehydrogenase Xq28 Blood Group Incompatibility,  Blackwater Fever,  Neonatal Jaundice,  Senile Cataract,  Glucosephosphate Dehydrogenase Deficiency,  Favism,  Hemolytic Anemia,  Mediterranean Spotted Fever,  Kernicterus,  Malaria Due To G6Pd Deficiency,  Diabetic Cataract,  Pyruvate Kinase Deficiency,  Malaria,  Aseptic Meningitis,  Ischemic Optic Neuropathy,  Congenital Hemolytic Anemia,  Methemoglobinemia,  Hepatitis A,  Gilbert Syndrome,  Anterior Ischemic Optic Neuropathy,  Color Blindness,  Acute Diarrhea,  Glucosephosphate Isomerase Deficiency,  Congenital Nonspherocytic Hemolytic Anemia,  Boutonneuse Fever,  Plasmodium Vivax Malaria,  Priapism,  Thalassemia,  Autoimmune Hemolytic Anemia,  Lysinuric Protein Intolerance,  Lead Poisoning,  Alpha Thalassemia,  Central Retinal Vein Occlusion,  Acute Chest Syndrome,  Parotitis,  Sickle Cell Disease,  Hereditary Elliptocytosis,  Congenital Methemoglobinemia,  Glutathione Synthetase Deficiency,  Viral Hepatitis,  Hyperphenylalaninemia,  Spotted Fever,  Plasmodium Falciparum Malaria Polycythemia Show all 44
GAA glucosidase, alpha; acid 17q25.3 Glycogen Storage Disease Ii,  Glycogen Storage Disease Due To Acid Maltase Deficiency, Juvenile Onset,  Glycogen Storage Disease Due To Acid Maltase Deficiency, Infantile Onset,  Glycogen Storage Disease Due To Acid Maltase Deficiency, Adult Onset,  Glycogen Storage Disease,  Danon Disease,  X-Linked Myopathy With Excessive Autophagy,  Respiratory Failure,  Vacuolar Myopathy,  Rippling Muscle Disease,  Krabbe Disease,  Carotid Artery Dissection,  Dysphagia,  Rigid Spine Syndrome Muscle Disorders Show all 15
GAB1 GRB2-associated binding protein 1 4q31.21 Leopard Syndrome
GABARAP GABA(A) receptor-associated protein 17p13.1 Stiff-Person Syndrome
GABARAPL1 GABA(A) receptor-associated protein like 1 12p13.2 Spastic Hemiplegia
GABBR1 gamma-aminobutyric acid (GABA) B receptor, 1 6p22.1 Persistent Vegetative State,  Multiple Sclerosis,  Withdrawal Disorder,  Schizophrenia,  Olivopontocerebellar Atrophy,  Reflex Sympathetic Dystrophy,  Sensory Neuropathy Type 1,  Temporal Lobe Epilepsy,  Tetanus Seasonal Affective Disorder Show all 10
GABBR2 gamma-aminobutyric acid (GABA) B receptor, 2 9q22.33 Nicotine Dependence,  Nicotine Addiction,  Nicotine Dependence, Protection Against,  Nicotine Addiction, Protection From Sensory Neuropathy Type 1 Show all 5
GABPA GA binding protein transcription factor, alpha subunit 60kDa 21q21.3 Down Syndrome
GABPB1 GA binding protein transcription factor, beta subunit 1 15q21.2 Adenylosuccinate Lyase Deficiency
GABRA1 gamma-aminobutyric acid (GABA) A receptor, alpha 1 5q34 Epilepsy, Childhood Absence, Susceptibility To, 4,  Epileptic Encephalopathy, Early Infantile, 19,  Epilepsy, Juvenile Myoclonic 5,  Gabra1-Related Juvenile Myoclonic Epilepsy,  Childhood Absence Epilepsy,  Dravet Syndrome,  Juvenile Myoclonic Epilepsy,  Juvenile Absence Epilepsy,  Early Myoclonic Encephalopathy Epilepsy, Childhood Absence, Susceptibility To, 2 Show all 10
GABRA2 gamma-aminobutyric acid (GABA) A receptor, alpha 2 4p12 Alcohol Dependence Cannabis Dependence
GABRA3 gamma-aminobutyric acid (GABA) A receptor, alpha 3 Xq28 Thyrotoxic Periodic Paralysis 1 Color Blindness
GABRA5 gamma-aminobutyric acid (GABA) A receptor, alpha 5 15q12 Angelman Syndrome Prader-Willi Syndrome
GABRA6 gamma-aminobutyric acid (GABA) A receptor, alpha 6 5q34 Heroin Dependence,  Alcohol Dependence,  Antisocial Personality Disorder,  Nicotine Addiction Asperger Syndrome Show all 5
GABRB1 gamma-aminobutyric acid (GABA) A receptor, beta 1 4p12 Schizophrenia
GABRB2 gamma-aminobutyric acid (GABA) A receptor, beta 2 5q34 Antisocial Personality Disorder
GABRB3 gamma-aminobutyric acid (GABA) A receptor, beta 3 15q12 Childhood Disintegrative Disease,  Epilepsy, Childhood Absence, Susceptibility To, 5,  Pervasive Developmental Disorder,  Prader-Willi Syndrome,  Angelman Syndrome,  Atypical Autism,  Diaphragmatic Eventration,  Post-Traumatic Stress Disorder,  Epilepsy, Childhood Absence, Susceptibility To, 2,  Childhood Absence Epilepsy Juvenile Absence Epilepsy Show all 11
GABRD gamma-aminobutyric acid (GABA) A receptor, delta 1p36.33 1P36 Deletion Syndrome,  Epilepsy, Generalized, With Febrile Seizures Plus, Type 5,  Epilepsy, Idiopathic Generalized, 10,  Gabrd-Related Generalized Epilepsy With Febrile Seizures Plus,  Gabrd-Related Juvenile Myoclonic Epilepsy,  Juvenile Myoclonic Epilepsy,  Generalized Epilepsy With Febrile Seizures Plus,  Febrile Seizures,  Focal Epilepsy,  Mood Disorder,  Nicotine Addiction,  Epilepsy, Generalized, With Febrile Seizures Plus, Type 1,  Dravet Syndrome Idiopathic Generalized Epilepsy Show all 14
GABRG2 gamma-aminobutyric acid (GABA) A receptor, gamma 2 5q34 Febrile Seizures, Familial, 8,  Psychomotor Disease,  Febrile Seizures,  Epilepsy, Childhood Absence, Susceptibility To, 2,  Epilepsy, Generalized, With Febrile Seizures Plus, Type 3,  Gabrg2-Related Generalized Epilepsy With Febrile Seizures Plus,  Gabrg2-Related Dravet Syndrome,  Generalized Epilepsy With Febrile Seizures Plus,  Myoclonic Epilepsy Of Infancy,  Epilepsy, Generalized, With Febrile Seizures Plus, Type 1,  Dravet Syndrome,  Juvenile Absence Epilepsy,  Childhood Absence Epilepsy Hyperekplexia Show all 14
GAD1 glutamate decarboxylase 1 (brain, 67kDa) 2q31.1 West Nile Fever,  Conversion Disorder,  Spastic Cerebral Palsy,  Peripheral Vertigo,  Limbic Encephalitis,  Cerebral Palsy, Spastic Quadriplegic, 1,  Stiff-Person Syndrome,  Rasmussen Encephalitis,  Type 1 Diabetes Mellitus,  Childhood-Onset Schizophrenia,  Pyridoxine-Dependent Epilepsy,  Diabetic Ketoacidosis,  Status Epilepticus,  Cerebral Palsy,  Encephalitis,  Schizophrenia,  Maternally Inherited Diabetes And Deafness Diabetic Retinopathy Show all 18
GAD2 glutamate decarboxylase 2 (pancreatic islets and brain, 65kDa) 10p12.1 Autoimmune Polyglandular Syndrome Type 2,  Congenital Rubella,  Spastic Cerebral Palsy,  Stiff-Person Syndrome,  Rubella,  Limbic Encephalitis,  Schizophrenia,  Diabetic Ketoacidosis,  Type 1 Diabetes Mellitus,  Obesity Cerebral Palsy Show all 11
GADD45A growth arrest and DNA-damage-inducible, alpha 1p31.3 Pancreatic Cancer,  Breast Cancer,  Ovarian Cancer,  Oral Cancer Schizophrenia Show all 5
GADD45B growth arrest and DNA-damage-inducible, beta 19p13.3 Liver Cancer
GAEC1 gene amplified in esophageal cancer 1 7q22.1 Esophageal Squamous Cell Carcinoma Esophageal Cancer
GAGE1 G antigen 1 Xp11.23 Glioblastoma Multiforme Stomach Cancer
GAGE12I G antigen 12I Xp11.23 Glioblastoma Multiforme
GAL galanin/GMAP prepropeptide 11q13.3 Normal Pressure Hydrocephalus,  Pain Disorder,  Mononeuropathy,  Hyperprolactinemia,  Seasonal Affective Disorder,  Acromegaly,  Ganglioneuroma,  Chronic Pain,  Narcolepsy,  Anorexia Nervosa Alzheimers Disease Show all 11
GAL3ST1 galactose-3-O-sulfotransferase 1 22q12.2 Renal Cell Carcinoma Metachromatic Leukodystrophy
GALC galactosylceramidase 14q31.3 Infantile Krabbe Disease,  Krabbe Disease,  Adult Krabbe Disease,  Late-Infantile/juvenile Krabbe Disease,  Leukodystrophy,  Metachromatic Leukodystrophy,  Lipid Storage Disease Gangliosidosis Show all 8
GALE UDP-galactose-4-epimerase 1p36.11 Epimerase Deficiency Galactosemia,  Erythrocyte Galactose Epimerase Deficiency,  Generalized Galactose Epimerase Deficiency,  Galactosemia,  Haemophilus Influenzae Typhoid Fever Show all 6
GALK1 galactokinase 1 17q25.1 Galactokinase Deficiency With Cataracts,  Galactokinase Deficiency,  Epimerase Deficiency Galactosemia,  Galactosemia,  Burkitts Lymphoma,  Mevalonic Aciduria Citrin Deficiency Show all 7
GALK2 galactokinase 2 15q21.1 Galactokinase Deficiency
GALNS galactosamine (N-acetyl)-6-sulfate sulfatase 16q24.3 Mucopolysaccharidosis Iv,  Kniest Dysplasia,  Mucopolysaccharidosis Vi,  Gangliosidosis,  Spondyloepiphyseal Dysplasia Congenita,  Larsen Syndrome,  Beta-Ketothiolase Deficiency,  Mucopolysaccharidosis Ketothiolase Deficiency Show all 9
GALNT11 :polypeptide N-acetylgalactosaminyltransferase 11 7q36.1 Heterotaxy
GALNT12 polypeptide N-acetylgalactosaminyltransferase 12 9q22.33 Colorectal Cancer 1 Colorectal Cancer
GALNT13 polypeptide N-acetylgalactosaminyltransferase 13 2q23.3 Tricuspid Valve Insufficiency Osteochondrosis
GALNT15 polypeptide N-acetylgalactosaminyltransferase 15 3p25.1 Hypertension
GALNT3 polypeptide N-acetylgalactosaminyltransferase 3 2q24.3 Hyperostosis-Hyperphosphatemia Syndrome,  Hyperphosphatemic Familial Tumoral Calcinosis, Galnt3-Related,  Normophosphatemic Familial Tumoral Calcinosis,  Hyperphosphatemia,  Hyperphosphatemic Familial Tumoral Calcinosis,  Familial Tumoral Calcinosis,  Calcinosis,  Hyperostosis,  Testicular Microlithiasis Tumoral Calcinosis, Hyperphosphatemic Show all 10
GALNT5 polypeptide N-acetylgalactosaminyltransferase 5 2q24.1 Hereditary Multiple Exostoses Exostosis
GALT galactose-1-phosphate uridylyltransferase 9p13.3 Galactosemia,  Lens Subluxation,  Galactokinase Deficiency,  Mayer-Rokitansky-Kuster-Hauser Syndrome,  Epimerase Deficiency Galactosemia Ovarian Cancer Show all 6
GAMT guanidinoacetate N-methyltransferase 19p13.3 Guanidinoacetate Methyltransferase Deficiency,  Cerebral Creatine Deficiency Syndrome,  Movement Disease,  Hypotonia,  Creatine Transporter Deficiency,  Creatine Deficiency Syndromes Agat Deficiency Show all 7
GAN gigaxonin 16q23.2 Endometriosis Of Uterus,  Giant Axonal Neuropathy,  Axonal Neuropathy,  Neuropathy Neuroaxonal Dystrophy Show all 5
GANAB glucosidase, alpha; neutral AB 11q12.3 Glycogen Storage Disease Ii Polycystic Liver Disease
GANC glucosidase, alpha; neutral C 15q15.1 Glycogen Storage Disease Ii Congenital Dyserythropoietic Anemia Type I
GAP43 growth associated protein 43 3q13.31 Appendicitis,  Status Epilepticus,  Cystitis,  Retinal Detachment Schizophrenia Show all 5
GAPDH glyceraldehyde-3-phosphate dehydrogenase 12p13.31 Diffuse Large B-Cell Lymphoma,  Obesity,  Plexiform Neurofibroma,  Pituitary Adenoma,  Parainfluenza Virus Type 3,  Turcot Syndrome,  Osteochondritis Dissecans,  Sleeping Sickness Acth-Secreting Pituitary Adenoma Show all 9
GAR1 GAR1 ribonucleoprotein 4q25 Aplastic Anemia Alcohol Dependence
GARS glycyl-tRNA synthetase 7p14.3 Charcot-Marie-Tooth Neuropathy Type 2D,  Distal Spinal Muscular Atrophy, Type V,  Charcot-Marie-Tooth Disease Type 2D,  Gars-Associated Axonal Neuropathy,  Distal Hereditary Motor Neuropathy Type V,  Neuropathy, Distal Hereditary Motor, Type Va,  Dermatomyositis,  Polymyositis,  Bscl2-Related Neurologic Disorders/seipinopathy,  Neuropathy,  Hyperekplexia,  Charcot-Marie-Tooth Neuropathy Type 2,  Distal Hereditary Motor Neuropathy,  Charcot-Marie-Tooth Disease Type 2 Spinal Muscular Atrophy Show all 15
GART phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase 21q22.11 Benign Mesothelioma
GAS1 growth arrest-specific 1 9q21.33 Basal Cell Carcinoma,  Nevoid Basal Cell Carcinoma Syndrome,  Septopreoptic Holoprosencephaly,  Midline Interhemispheric Variant Of Holoprosencephaly,  Pallister-Hall Syndrome,  Alobar Holoprosencephaly,  Lobar Holoprosencephaly,  Melanoma Metastasis,  Single Median Maxillary Central Incisor Semilobar Holoprosencephaly Show all 10
GAS2 growth arrest-specific 2 11p14.3 Gnathodiaphyseal Dysplasia
GAS6 growth arrest-specific 6 13q34 Limb Ischemia,  Critical Limb Ischemia,  Ocular Melanoma Demyelinating Polyneuropathy Show all 4
GAS7 growth arrest-specific 7 17p13.1 Spastic Hemiplegia
GAST gastrin 17q21.2 Gastric Mucosal Hypertrophy,  Collagenous Gastritis,  Ovarian Mucinous Cystadenocarcinoma,  Gastric Endocrine Tumor,  Duodenitis,  Gastroduodenitis,  Pancreatic Cancer,  Mucinous Cystadenocarcinoma,  Postcholecystectomy Syndrome,  Ostertagiasis,  Megaesophagus,  Pernicious Anemia,  Gastric Outlet Obstruction,  Duodenal Gastrinoma,  Apudoma,  Pancreatic Gastrinoma,  Somatostatinoma,  Zollinger-Ellison Syndrome,  Goblet Cell Carcinoid,  Familial Isolated Hyperparathyroidism,  Biliary Tract Disease,  Diabetic Autonomic Neuropathy,  Duodenogastric Reflux,  Vipoma,  Serotonin Syndrome,  Gastritis,  Cardia Cancer,  Wermer Syndrome,  Pancreatic Islet Cell Tumors,  Megacolon Carcinoid Syndrome Show all 31
GATA1 GATA binding protein 1 (globin transcription factor 1) Xp11.23 Thrombocytopenia With Beta-Thalassemia, X-Linked,  Gata1-Related X-Linked Cytopenia,  Gata1-Related Cytopenia,  Acute Megakaryoblastic Leukemia In Down Syndrome,  Dyserythropoietic Anemia And Thrombocytopenia,  Tetrasomy 21,  Thrombocytopenia, X-Linked, With Or Without Dyserythropoietic Anemia,  Leukemia, Megakaryoblastic, With Or Without Down Syndrome, Somatic,  Anemia, X-Linked, With/without Neutropenia And/or Platelet Abnormalities,  Gata1-Related Diamond-Blackfan Anemia,  Acute Basophilic Leukemia,  Thrombocytopenia,  X-Linked Thrombocytopenia,  Gray Platelet Syndrome,  Congenital Erythropoietic Porphyria,  Leukemoid Reaction,  Megakaryocytic Leukemia,  Myelofibrosis,  Hereditary Persistence Of Fetal Hemoglobin,  Congenital Porphyria,  Thalassemia,  Myelodysplastic Syndromes,  Diamond-Blackfan Anemia 1 Acute Myeloid Leukemia Show all 24
GATA2 GATA binding protein 2 3q21.3 Lymphedema, Primary, With Myelodysplasia,  Emberger Syndrome,  Immunodeficiency 21,  Myelodysplastic Syndromes,  Myelodysplastic Syndrome, Susceptibility, Gata2-Related,  Acute Myeloid Leukemia, Susceptibility, Gata2-Related,  Dendritic Cell, Monocyte, B Lymphocyte, And Natural Killer Lymphocyte Deficiency,  Acute Myeloid Leukemia,  Myelodysplastic Syndrome, Somatic Aplastic Anemia Show all 10
GATA3 GATA binding protein 3 10p14 Hypoparathyroidism, Sensorineural Deafness, And Renal Disease,  Renal Dysplasia,  Barakat Syndrome,  Sarcomatoid Renal Cell Carcinoma,  Hypoparathyroidism,  Nephritis,  Acute Lymphoblastic Leukemia,  Leukemia, Acute Lymphoblastic 3 Breast Cancer Show all 9
GATA4 GATA binding protein 4 8p23.1 Atrioventricular Septal Defect 4,  Chromosome 8P23.1 Deletion,  Testicular Anomalies With Or Without Congenital Heart Disease,  Ventricular Septal Defect 1,  Pyromania,  Atrial Septal Defect 2,  8P23.1 Duplication Syndrome,  Partial Atrioventricular Canal,  Complete Atrioventricular Canal - Ventricle Hypoplasia,  Complete Atrioventricular Canal - Left Heart Obstruction,  Single Ventricular Septal Defect,  Complete Atrioventricular Canal - Fallot Tetralogy,  Atrioventricular Septal Defect,  Congenital Heart Disease,  Patent Foramen Ovale,  46Xy Sex Reversal 2, Dosage-Sensitive,  Tetralogy Of Fallot,  Tetrology Of Fallot,  Ovarian Germ Cell Tumor,  Ventricular Septal Defect,  Atrial Fibrillation, Familial, 3,  Ebstein Anomaly,  Transposition Of The Great Arteries,  Familial Atrial Fibrillation,  Atrioventricular Block Double Outlet Right Ventricle Show all 26
GATA5 GATA binding protein 5 20q13.33 Aortic Valve Disease,  Single Ventricular Septal Defect,  Familial Atrial Fibrillation,  Tetralogy Of Fallot Atrial Fibrillation, Familial, 3 Show all 5
GATA6 GATA binding protein 6 18q11.2 Atrial Septal Defect 9,  Atrioventricular Septal Defect 5,  Pancreatic Agenesis And Congenital Heart Defects,  Ovarian Germ Cell Tumor,  Atrioventricular Septal Defect,  Tetralogy Of Fallot,  Persistent Truncus Arteriosus,  Patent Foramen Ovale,  Atrial Septal Defect 2,  Pancreatic Agenesis,  Velocardiofacial Syndrome,  Partial Atrioventricular Canal,  Tetrology Of Fallot,  Familial Atrial Fibrillation,  Complete Atrioventricular Canal - Ventricle Hypoplasia,  Double Outlet Right Ventricle,  Conotruncal Heart Malformations, Variable,  Atrial Fibrillation, Familial, 3,  Conotruncal Heart Malformations Diaphragmatic Hernia 3 Show all 20
GATAD1 GATA zinc finger domain containing 1 7q21.2 Cardiomyopathy, Dilated, 2B,  Cardiomyopathy, Dilated, 1Ii Dilated Cardiomyopathy
GATAD2B GATA zinc finger domain containing 2B 1q21.3 Mental Retardation, Autosomal Dominant 18
GATM glycine amidinotransferase (L-arginine:glycine amidinotransferase) 15q21.1 Renal Tuberculosis,  Agat Deficiency,  Cerebral Creatine Deficiency Syndrome,  Diffuse Glomerulonephritis,  Creatine Transporter Deficiency,  Creatine Deficiency Syndromes Acute Pancreatitis Show all 7
GBA glucosidase, beta, acid 1q22 Gaucher Disease Perinatal Lethal,  Gaucher Disease Type 2,  Gaucher Disease Type 1,  Lewy Body Dementia,  Parkinson Disease, Late-Onset,  Gaucher Disease Type 3,  Gaucher Disease, Type Iiic,  Gauchers Disease,  Cholesteryl Ester Storage Disease,  Corticobasal Degeneration,  Adenosine Deaminase Deficiency,  Splenomegaly,  Chitotriosidase Deficiency,  Hypersplenism,  Parkinsons Disease,  Lrrk2-Related Parkinson Disease,  Prolidase Deficiency,  Lysosomal Storage Disease,  Pancytopenia,  Hypoalphalipoproteinemia,  Parkinson Disease Type 9,  Fabry Disease Parkinson Disease 1 Show all 23
GBA2 glucosidase, beta (bile acid) 2 9p13.3 Spastic Paraplegia 46, Autosomal Recessive,  Splenic Sequestration,  Autosomal Recessive Cerebellar Ataxia With Late-Onset Spasticity Spasticity Show all 4
GBA3 glucosidase, beta, acid 3 (gene/pseudogene) 4p15.2 Gauchers Disease
GBAS glioblastoma amplified sequence 7p11.2 Glioblastoma
GBD2 gallbladder disease 2 1p36.21 Gallbladder Disease 2 Gallbladder Disease
GBD3 gallbladder disease 3 1p34.3 Gallbladder Disease 3 Gallbladder Disease
GBE1 glucan (1,4-alpha-), branching enzyme 1 3p12.2 Adult Polyglucosan Body Disease,  Glycogen Storage Disease Iv,  Gbe1-Related Disorders,  Sea-Blue Histiocyte Syndrome,  Glycogen Storage Disease Lafora Disease Show all 6
GBP1 guanylate binding protein 1, interferon-inducible 1p22.2 Pseudopseudohypoparathyroidism,  Aneurysmal Bone Cysts Chronic Active Epstein-Barr Virus Infection
GBP3 guanylate binding protein 3 1p22.2 Hypoglycemic Coma
GBP5 guanylate binding protein 5 1p22.2 Chronic Active Epstein-Barr Virus Infection
GBX2 gastrulation brain homeobox 2 2q37.2 Prostate Cancer
GC group-specific component (vitamin D binding protein) 4q13.3 Graves Disease,  Tuberculosis,  Osteoporosis,  Nervous System Disease,  Acute Liver Failure Central Nervous System Disease Show all 6
GC06M011196 Non-Small Cell Lung Carcinoma
GC07P072301 Shwachman-Diamond Syndrome
GCC1 GRIP and coiled-coil domain containing 1 7q32.1 Secretory Diarrhea
GCC2 GRIP and coiled-coil domain containing 2 2q12.3 Secretory Diarrhea
GCCD2 Glucocorticoid deficiency 2 Glucocorticoid Deficiency 2,  Glucocorticoid Deficiency 3 Familial Glucocorticoid Deficiency
GCCD3 glucocorticoid deficiency 3 8q11.2-q13.2 Glucocorticoid Deficiency 3 Familial Glucocorticoid Deficiency
GCDH glutaryl-CoA dehydrogenase 19p13.2 Glutaric Acidemia Type I,  Athetosis,  Organic Acidemia,  The Organic Acidemias: An,  Generalized Dystonia,  Movement Disease,  L-2-Hydroxyglutaric Aciduria,  2-Hydroxyglutaric Aciduria D-2-Hydroxyglutaric Aciduria Show all 9
GCG glucagon 2q24.2 Type 2 Diabetes Mellitus,  Obesity,  Dumping Syndrome,  Glossitis,  Steatorrhea,  Diabetic Autonomic Neuropathy,  Somatostatinoma,  Acute Insulin Response Intestinal Disease Show all 9
GCGR glucagon receptor 17q25.3 Insulin Resistance,  Diabetes Mellitus, Noninsulin-Dependent, 2,  Diabetes Mellitus, Noninsulin-Dependent, Late Onset,  Diabetes Mellitus, Type 2, Susceptiblity To,  Diabetes Mellitus, Noninsulin-Dependent, Association With,  Hypertension, Insulin Resistance-Related,  Diabetes Mellitus, Noninsulin-Dependent,  Type 2 Diabetes Mellitus,  Essential Hypertension,  Diabetes Mellitus,  Pheochromocytoma Hyperglycemia Show all 12
GCH1 GTP cyclohydrolase 1 14q22.2 Gtp Cyclohydrolase 1-Deficient Dopa-Responsive Dystonia,  Oromandibular Dystonia,  Dystonia 14,  Gtp Cyclohydrolase I Deficiency,  Dopa-Responsive Dystonia Multi-Gene Panels,  Dystonia 5, Dopa-Responsive Type,  Dystonia, Dopa-Responsive, With Or Without Hyperphenylalaninemia,  Gtp Cyclohydrolase 1-Related Disorders,  Dystonia,  Hyperphenylalaninemia,  Torsion Dystonia,  Somatoform Disorder,  Cervical Dystonia,  Tyrosine Hydroxylase Deficiency,  Tetrahydrobiopterin Deficiency,  Myoclonus-Dystonia,  Degenerative Disc Disease,  Low Renin Hypertension,  Movement Disease,  Parkinsons Disease Vitiligo Show all 21
GCK glucokinase (hexokinase 4) 7p13 Chromosome 7P Deletion,  Maturity-Onset Diabetes Of The Young,  Gestational Diabetes,  Diabetes Mellitus, Noninsulin-Dependent, Late Onset,  Gck-Related Hyperinsulinism,  Hyperinsulinemic Hypoglycemia Familial 3,  Maturity-Onset Diabetes Of The Young, Type 2,  Gck-Related Permanent Neonatal Diabetes Mellitus,  Hypoglycemia,  Permanent Neonatal Diabetes Mellitus,  Maturity-Onset Diabetes Of The Young, Type 1,  Diabetes Mellitus,  Monogenic Diabetes,  Diabetes Mellitus, Permanent Neonatal, With Neurologic Features,  Familial Hyperinsulinism,  Hyperglycemia,  Hyperinsulinemic Hypoglycemia,  Hyperinsulinism,  3-Hydroxyacyl-Coa Dehydrogenase Deficiency,  Leucine-Sensitive Hypoglycemia Of Infancy,  Greig Cephalopolysyndactyly Syndrome,  Pancreatic Agenesis,  Type 2 Diabetes Mellitus Insulinoma Show all 24
GCKR glucokinase (hexokinase 4) regulator 2p23.3 Maturity-Onset Diabetes Of The Young Cardiovascular Disease Risk Factor
GCLC glutamate-cysteine ligase, catalytic subunit 6p12.1 Hemolytic Anemia Due To Gamma-Glutamylcysteine Synthetase Deficiency,  Myocardial Infarction,  Cisplatin Toxicity Hemolytic Anemia Show all 4
GCLM glutamate-cysteine ligase, modifier subunit 1p22.1 Myocardial Infarction Ischemic Heart Disease
GCM2 glial cells missing homolog 2 (Drosophila) 6p24.2 Hypoparathyroidism Familial Isolated,  Gcm2-Related Familial Isolated Hypoparathyroidism,  Familial Isolated Hypoparathyroidism Due To Agenesis Of Parathyroid Gland,  Hypoparathyroidism,  Primary Hyperparathyroidism,  Hypoparathyroidism, Autosomal Recessive Hypoparathyroidism, Autosomal Dominant Show all 7
GCNT1 glucosaminyl (N-acetyl) transferase 1, core 2 9q21.13 Mast Cell Neoplasm
GCNT2 glucosaminyl (N-acetyl) transferase 2, I-branching enzyme (I blood group) 6p24.3 Adult I Phenotype Without Cataract,  Cataract 13 With Adult I Phenotype,  Ophthalmia Neonatorum,  Adult I Blood Group With Or Without Congenital Cataract,  Cataract, Congenital,  Mast Cell Neoplasm,  Brain Disease Cataract Show all 8
GCNT4 glucosaminyl (N-acetyl) transferase 4, core 2 5q13.3 Mast Cell Neoplasm
GCSAM germinal center-associated, signaling and motility 3q13.2 Diffuse Large B-Cell Lymphoma
GCSH glycine cleavage system protein H (aminomethyl carrier) 16q23.2 Atypical Glycine Encephalopathy,  Neonatal Glycine Encephalopathy,  Infantile Glycine Encephalopathy,  Gcsh-Related Glycine Encephalopathy,  Glycine Encephalopathy Desquamative Interstitial Pneumonia Show all 6
GDAP1 ganglioside induced differentiation associated protein 1 8q21.11 Charcot-Marie-Tooth Disease, Axonal, With Vocal Cord Paresis,  Charcot-Marie-Tooth Neuropathy Type 4A,  Charcot-Marie-Tooth Disease Type 2G,  Charcot-Marie-Tooth Disease Type 2H,  Gdap1-Related Intermediate Charcot-Marie-Tooth Neuropathy,  Charcot-Marie-Tooth Disease, Recessive Intermediate, A,  Charcot-Marie-Tooth Disease Type 2K,  Charcot-Marie-Tooth Neuropathy Type 2H/2K,  Tooth Disease,  Neuropathy,  Charcot-Marie-Tooth Neuropathy Type 2,  Charcot-Marie-Tooth Neuropathy Type 4,  Charcot-Marie-Tooth Disease,  Charcot-Marie-Tooth Disease Type 2,  Charcot-Marie-Tooth Disease Type 4,  Clubfoot Mitochondrial Complex I Deficiency Show all 17
GDAP1L1 ganglioside induced differentiation associated protein 1-like 1 20q13.12 Neuroblastoma
GDF1 growth differentiation factor 1 19p13.11 Right Atrial Isomerism,  Double Outlet Right Ventricle,  Transposition Of Great Arteries, Dextro-Looped 3,  Tetralogy Of Fallot,  Transposition Of The Great Arteries,  Conotruncal Heart Malformations,  Velocardiofacial Syndrome,  Klippel-Feil Syndrome,  Ventricular Septal Defect,  Persistent Truncus Arteriosus,  Conotruncal Heart Malformations, Variable,  Transposition Of The Great Arteries, Dextro-Looped 1 Tetrology Of Fallot Show all 13
GDF10 growth differentiation factor 10 10q11.22 Osteosarcoma
GDF15 growth differentiation factor 15 19p13.11 Pyruvate Kinase Deficiency,  Oral Cavity Cancer,  Congenital Dyserythropoietic Anemia Type I,  Estrogen Resistance,  Prostatitis,  Anoxia Prostate Cancer Show all 7
GDF2 growth differentiation factor 2 10q11.22 Telangiectasia, Hereditary Hemorrhagic, Type 5,  Hereditary Hemorrhagic Telangiectasia Hepatopulmonary Syndrome
GDF3 growth differentiation factor 3 12p13.31 Microphthalmia With Coloboma 6,  Klippel-Feil Syndrome 3, Autosomal Dominant,  Microphthalmia, Isolated 7,  Klippel-Feil Syndrome,  Coloboma,  Mixed Germ Cell Tumor,  Microphthalmia With Coloboma 6, Digenic,  Microphthalmia, Isolated, With Coloboma 7 Microphthalmia Show all 9
GDF5 growth differentiation factor 5 20q11.22 Fibular Hypoplasia And Complex Brachydactyly,  Multiple Synostoses Syndrome 2,  Fibular Hypoplasia,  Osteoarthritis-5,  Acromesomelic Dysplasia, Hunter-Thompson Type,  Brachydactyly Type C,  Brachydactyly Type A2,  Brachydactyly,  Acromesomelic Dysplasia, Grebe Type,  Symphalangism, Proximal, 1B,  Brachydactyly, Type A1, C,  Angel Shaped Phalangoepiphyseal Dysplasia,  Acromesomelic Dysplasia,  Brachydactyly Type A1,  Multiple Synostoses Syndrome,  Spondylolisthesis,  Ankylosis,  Proximal Symphalangism,  Degenerative Disc Disease,  Root Resorption,  Multiple Synostosis Syndrome 1 Chondrodysplasia Show all 22
GDF6 growth differentiation factor 6 8q22.1 Klippel-Feil Syndrome 1, Autosomal Dominant,  Leber Congenital Amaurosis 17,  Segmentation Syndrome 1,  Klippel-Feil Syndrome,  Microphthalmia With Coloboma 6, Digenic,  Microphthalmia, Isolated 4,  Coloboma,  Leber Congenital Amaurosis 10,  Klippel-Feil Syndrome 3, Autosomal Dominant Microphthalmia, Isolated, With Coloboma 7 Show all 10
GDF7 growth differentiation factor 7 2p24.1 Ankylosis
GDF9 growth differentiation factor 9 5q31.1 Kidney Cancer,  Polycystic Ovary Syndrome Premature Ovarian Failure
GDI1 GDP dissociation inhibitor 1 Xq28 Tumor Of Exocrine Pancreas,  Mental Retardation Mental Retardation, X-Linked 29 And Others
GDNF glial cell derived neurotrophic factor 5p13.2 Central Hypoventilation Syndrome,  Spinal Cord Injury,  Intestinal Obstruction,  Pheochromocytoma, Modifier Of,  Hirschsprung Disease Type 3,  Gdnf-Related Hirschsprung Disease,  Hirschsprungs Disease,  Neuroma,  Medullary Sponge Kidney,  Dry Eye Syndrome,  Pheochromocytoma,  Multiple Endocrine Neoplasia Type 2A,  Sacrococcygeal Teratoma,  Congenital Central Hypoventilation Syndrome,  Brain Injury,  Spinal Cord Disease,  Familial Medullary Thyroid Carcinoma,  Pyloric Stenosis,  Pancreatic Cancer,  Hereditary Paraganglioma-Pheochromocytoma Syndromes,  Hypertrophic Pyloric Stenosis,  Cerebral Artery Occlusion,  Brain Ischemia,  Parkinsons Disease,  Multiple Endocrine Neoplasia,  Renal Agenesis,  Central Hypoventilation Syndrome, Congenital, With Or Without Hirschsprung Disease,  Polyneuropathy Ischemia Show all 29
GEFSP4 Epilepsy, generalized, with febrile seizures plus, type 4 2p24 Epilepsy, Generalized, With Febrile Seizures Plus, Type 4
GEFSP6 Generalized epilepsy with febrile seizures plus, type 6 8p23-p21 Epilepsy, Generalized, With Febrile Seizures Plus, Type 6 Generalized Epilepsy With Febrile Seizures Plus
GEFSP8 Generalized epilepsy with febrile seizures plus, type 8 6q16.3-q22.31 Epilespy, Generalized, With Febrile Seizures Plus, Type 8 Generalized Epilepsy With Febrile Seizures Plus
GEMIN2 gem (nuclear organelle) associated protein 2 14q21.1 Mowat-Wilson Syndrome Benign Hereditary Chorea
GER Gastroesophageal reflux 13q14 Gastroesophageal Reflux Disease
GET4 golgi to ER traffic protein 4 homolog (S. cerevisiae) 7p22.3 Louping Ill Erysipeloid
GFAP glial fibrillary acidic protein 17q21.31 Papillary Ependymoma,  Ring Chromosome 7,  Astroblastoma,  Mixed Glioma,  Epithelial-Myoepithelial Carcinoma,  Alexander Disease,  Neuroectodermal Tumor,  Gliomatosis Cerebri,  Oligodendroglioma,  Alexander Disease Type Ii,  Alexander Disease Type I,  Oligoastrocytoma,  Binswangers Disease,  Astrocytoma,  Melanotic Neuroectodermal Tumor,  Gemistocytic Astrocytoma,  Ganglioglioma,  Ependymoma,  Glioblastoma,  Subependymal Giant Cell Astrocytoma,  Pleomorphic Xanthoastrocytoma,  Malignant Glioma,  Ependymoblastoma,  Psammomatous Meningioma,  Pituicytoma,  Myxopapillary Ependymoma,  Central Neurocytoma,  Meningioma,  Syringoma,  Anaplastic Ependymoma,  Normal Pressure Hydrocephalus,  Medulloblastoma,  Subcortical Arteriosclerotic Encephalopathy,  Chordoid Glioma,  Tanycytic Ependymoma,  Suprasellar Meningioma,  Papillary Glioneuronal Tumor,  Cellular Schwannoma,  Pineoblastoma,  Glioblastoma Multiforme,  Fetal Alcohol Syndrome,  Cerebellar Medulloblastoma,  Pilomyxoid Astrocytoma,  Sleeping Sickness,  Chordoid Meningioma,  Tuberous Sclerosis,  Sacrococcygeal Teratoma,  Pediatric Ependymoma,  Chondroblastic Osteosarcoma,  Pituitary Carcinoma,  Dysembryoplastic Neuroepithelial Tumor,  Pineocytoma,  Pilocytic Astrocytoma,  Extraventricular Neurocytoma,  Angiocentric Glioma,  Gliosarcoma,  Neurilemmoma,  Mesenchymal Chondrosarcoma,  Traumatic Brain Injury,  Giant Cell Glioblastoma,  Chordoma,  Ossifying Fibroma,  Choroid Plexus Papilloma,  Teratoma,  Medulloblastoma, Desmoplastic,  Myoepithelioma,  Cerebral Atrophy,  Retinal Detachment,  Proliferative Vitreoretinopathy,  Hereditary Cerebral Hemorrhage With Amyloidosis,  Macular Holes,  Anaplastic Oligodendroglioma,  Blastoma Head Injury Show all 74
GFER growth factor, augmenter of liver regeneration 16p13.3 Nodular Regenerative Hyperplasia,  Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay,  Polycystic Kidney Disease Kidney Disease Show all 4
GFI1 growth factor independent 1 transcription repressor 1p22.1 Severe Congenital Neutropenia,  Neutropenia,  Idiopathic Neutropenia,  Tetraploidy,  Severe Congenital Neutropenia, Autosomal Dominant, 2,  Reticular Dysgenesis Splenic Marginal Zone Lymphoma Show all 7
GFI1B growth factor independent 1B transcription repressor 9q34.13 Bleeding Disorder, Platelet-Type, 17,  Gray Platelet Syndrome,  Megakaryocytic Leukemia,  Reticular Dysgenesis,  Aplastic Anemia Chronic Leukemia Show all 6
GFM1 G elongation factor, mitochondrial 1 3q25.32 Combined Oxidative Phosphorylation Deficiency 1,  Heart Aneurysm,  Factor Vii Deficiency Pearson Syndrome Show all 4
GFM2 G elongation factor, mitochondrial 2 5q13.3 Atorvastatin Toxicity
GFND1 Glomerulopathy with fibronectin deposits 1 1q32 Glomerulopathy With Fibronectin Deposits 1
GFPT1 glutamine--fructose-6-phosphate transaminase 1 2p13.3 Myasthenia, Congenital, With Tubular Aggregates 1,  Gfpt1-Related Congenital Myasthenic Syndrome,  Myasthenia, Limb-Girdle, With Tubular Aggregates Congenital Myasthenic Syndrome With Episodic Apnea Show all 4
GFRA1 GDNF family receptor alpha 1 10q25.3 Hirschsprungs Disease,  Multiple Endocrine Neoplasia Type 2A,  Central Hypoventilation Syndrome Congenital Central Hypoventilation Syndrome Show all 4
GFRA2 GDNF family receptor alpha 2 8p21.3 Hirschsprungs Disease
GGCX gamma-glutamyl carboxylase 2p11.2 Pseudoxanthoma Elasticum-Like Disorder With Multiple Coagulation Factor Deficiency,  Hemorrhagic Disease,  Vitamin K Deficiency Hemorrhagic Disease,  Vitamin K-Dependent Clotting Factors, Combined Deficiency Of, 1,  Pseudoxanthoma Elasticum Herpes Simplex Show all 6
GGH gamma-glutamyl hydrolase (conjugase, folylpolygammaglutamyl hydrolase) 8q12.3 Tropical Sprue,  Pulmonary Neuroendocrine Tumor,  Genital Herpes,  Neuroendocrine Tumor,  Herpes Simplex,  Methotrexate Dose Selection Acromegaly Show all 7
GGT1 gamma-glutamyltransferase 1 22q11.23 Glutathionuria,  Glutathioninuria,  Opisthorchiasis,  Aagenaes Syndrome,  Choledocholithiasis,  Primary Biliary Cirrhosis,  Fascioliasis,  Liver Disease,  Insulin Resistance,  Obesity,  Osteogenesis Imperfecta Type I,  Pleuropneumonia,  Hepatic Tuberculosis,  Glutathione Synthetase Deficiency,  Hepatitis B,  Nodular Regenerative Hyperplasia,  Extrahepatic Cholestasis,  Vulvovaginal Candidiasis,  Recessive Dystrophic Epidermolysis Bullosa,  Lead Poisoning,  Factor Vii Deficiency,  Tuberculous Meningitis,  Aortic Valve Disease,  Villous Adenoma,  Hypoalphalipoproteinemia Gallbladder Disease Show all 26
GGT3P gamma-glutamyltransferase 3 pseudogene 22q11.21 Benign Recurrent Intrahepatic Cholestasis,  Stickler Syndrome Hyperthyroxinemia
GGT6 gamma-glutamyltransferase 6 17p13.2 Glutathionuria
GGTA1P glycoprotein, alpha-galactosyltransferase 1 pseudogene 9q33.2 Germ Cell Tumors
GH1 growth hormone 1 17q23.3 Kowarski Syndrome,  Protein-Deficiency Anemia,  Isolated Growth Hormone Deficiency Type 2,  Marasmus,  Growth Hormone Deficiency,  Isolated Growth Hormone Deficiency Type 1A,  Isolated Growth Hormone Deficiency Type 1B,  Isolated Growth Hormone Deficiency, Type Ib, Gh1-Related,  Isolated Growth Hormone Deficiency,  Leptin Deficiency,  Fibrous Dysplasia,  Acromegaly,  Laron Syndrome,  Adenohypophysitis,  Hypoadrenalism,  Mccune Albright Syndrome,  Short Stature,  Pituitary Adenoma,  Gigantism,  Pituitary Apoplexy,  Nephropathic Cystinosis,  Somatostatin Analog,  Arachnoid Cysts,  Aromatase Deficiency,  Craniopharyngioma,  Vipoma,  Trophoblastic Neoplasm,  Hypersomnia,  Floating-Harbor Syndrome,  Rabson-Mendenhall Syndrome,  Syringomyelia,  Ovarian Disease,  Robinow Syndrome,  Tetrahydrobiopterin Deficiency,  Obesity,  Septo-Optic Dysplasia,  Pituitary Tumors,  Pituitary Hypoplasia,  Turner Syndrome,  Osteoporosis,  Acth Deficiency,  Adenoma,  Dwarfism Prader-Willi Syndrome Show all 44
GH2 growth hormone 2 17q23.3 Isolated Growth Hormone Deficiency,  Trophoblastic Neoplasm,  Pituitary Tumors Choriocarcinoma Show all 4
GHR growth hormone receptor 5p13.1 Papilledema,  Laron Syndrome,  Hypercholesterolemia, Familial, Modifier Of,  Increased Responsiveness To Growth Hormone,  Short Stature,  Actinic Keratosis,  Hypercholesterolemia,  Familial Hypercholesterolemia,  Bells Palsy,  Acromegaly,  Ldl Cholesterol Level Qtl2,  Coronary Artery Disease In Familial Hypercholesterolemia, Protection Against,  Plexiform Neurofibroma,  Hypercholesterolemia, Familial, Due To Ldlr Defect, Modifier Of,  Pituitary Adenoma,  Noonan Syndrome,  Insulin-Like Growth Factor I Deficiency,  Drug-Induced Hepatitis,  Isolated Growth Hormone Deficiency Osteoporosis Show all 20
GHRH growth hormone releasing hormone 20q11.23 Gigantism,  Isolated Growth Hormone Deficiency Due To Defect In Ghrf,  Gigantism Due To Ghrf Hypersecretion,  Carcinoid Syndrome,  Somatostatinoma,  Central Neurocytoma,  Vipoma,  Isolated Growth Hormone Deficiency,  Recessive Dystrophic Epidermolysis Bullosa,  Serotonin Syndrome,  Pituitary Carcinoma,  Zollinger-Ellison Syndrome,  Pancreatic Islet Cell Tumors,  Liver Cirrhosis,  Dwarfism,  Anorexia Nervosa,  Growth Hormone Deficiency,  Acromegaly,  Somatostatin Analog,  Pituitary Hypoplasia,  Panic Disorder,  Glucagonoma,  Hypopituitarism Obesity Show all 24
GHRHR growth hormone releasing hormone receptor 7p14.3 Pancreatic Islet Cell Tumors,  Isolated Growth Hormone Deficiency,  Isolated Growth Hormone Deficiency, Type Ib, Ghrhr-Related,  Pituitary Hypoplasia,  Growth Hormone Deficiency,  Dwarfism,  Prolactinoma,  Short Stature,  Isolated Growth Hormone Deficiency Type 2,  Pituitary Tumors,  Isolated Growth Hormone Deficiency Type 1B,  Acromegaly,  Somatostatin Analog Prostate Cancer Show all 14
GHRL ghrelin/obestatin prepropeptide 3p25.3 Gastric Endocrine Tumor,  Stomach Disease,  Gastroparesis,  Eating Disorder,  Obesity,  Gastritis,  Atrophic Gastritis,  Dyspepsia,  Anorexia Nervosa,  Autoimmune Atrophic Gastritis,  Gastrointestinal Neuroendocrine Tumor,  Bulimia Nervosa,  Intestinal Disease,  Prader-Willi Syndrome,  Insulin Resistance,  Polycystic Ovary Syndrome,  Acth-Secreting Pituitary Adenoma,  Type 2 Diabetes Mellitus,  Seizure Disorder,  Neuroendocrine Tumor,  Anovulation Peptic Ulcer Disease Show all 22
GHS Goldenhar syndrome Goldenhar Syndrome
GHSR growth hormone secretagogue receptor 3q26.31 Short Stature,  Partial Isolated Growth Hormone Deficiency,  Anorexia Nervosa,  Gastroparesis,  Isolated Growth Hormone Deficiency,  Obesity,  Growth Hormone Deficiency,  Acromegaly Cushings Syndrome Show all 9
GIF gastric intrinsic factor (vitamin B synthesis) 11q12.1 Congenital Intrinsic Factor Deficiency,  Blind Loop Syndrome,  Diphyllobothriasis,  Pernicious Anemia,  Intrinsic Factor Deficiency,  Transcobalamin Ii Deficiency,  Galactosemia,  Methylmalonic Aciduria And Homocystinuria Type Cblf,  Methylmalonic Aciduria And Homocystinuria Type Cble,  Methylmalonic Aciduria And Homocystinuria Type Cblg,  Methylmalonic Aciduria And Homocystinuria Type Cblc,  Methylmalonic Aciduria And Homocystinuria Type Cbld,  Vitamin B12 Deficiency,  Cblg,  Cble Megaloblastic Anemia Show all 16
GIGYF2 GRB10 interacting GYF protein 2 2q37.1 Parkinsons Disease,  Parkinson Disease 11 Parkinson Disease 1
GIMAP1 GTPase, IMAP family member 1 7q36.1 Breast And Colorectal Cancer
GIMAP4 GTPase, IMAP family member 4 7q36.1 Acute Lymphocytic Leukemia
GIMAP5 GTPase, IMAP family member 5 7q36.1 Systemic Lupus Erythematosus
GIMAP6 GTPase, IMAP family member 6 7q36.1 Lung Cancer
GIN1 gypsy retrotransposon integrase 1 5q21.1 Parametritis
GINGF2 gingival fibromatosis, hereditary, 2 5q13-q22 Gingival Fibromatosis, 2
GINGF3 Fibromatosis, gingival, 3 2p23.3-p22.3 Gingival Fibromatosis, 3 Fibromatosis, Gingival
GINGF4 gingival fibromatosis, hereditary, 4 11p15 Gingival Fibromatosis, 4
GIP gastric inhibitory polypeptide 17q21.32 Ventricular Tachycardia, Idiopathic,  Acth-Secreting Pituitary Adenoma,  Type 2 Diabetes Mellitus,  Cushings Syndrome,  Hyperglycemia,  Dumping Syndrome,  Somatostatinoma,  Insulin Resistance Obesity Show all 9
GIPC3 GIPC PDZ domain containing family, member 3 19p13.3 Deafness, Autosomal Recessive 15,  Audiogenic Seizures,  Sporadic Breast Cancer,  Autosomal Recessive Nonsyndromic Deafness,  Deafness, Digenic, Gjb2/gjb3 Nonsyndromic Deafness Show all 6
GIPR gastric inhibitory polypeptide receptor 19q13.32 Adrenal Cortical Adenoma,  Adrenal Adenoma,  Cushings Syndrome Insulinoma Show all 4
GJA1 gap junction protein, alpha 1, 43kDa 6q22.31 Criss-Cross Heart,  Atrioventricular Septal Defect 3,  Oculodentodigital Dysplasia, Autosomal Recessive,  Oculodentodigital Dysplasia,  Hypoplastic Left Heart Syndrome 1,  Hallermann-Streiff Syndrome,  Syndactyly,  Hypoplastic Left Heart Syndrome,  Syndactyly Type 3,  Atrioventricular Septal Defect,  Dental Enamel Hypoplasia,  Brain Glioma,  Heterotaxy,  Craniometaphyseal Dysplasia,  Axenfeld-Rieger Syndrome,  Keratosis Follicularis,  Hailey-Hailey Disease,  Dilated Cardiomyopathy,  Skin Atrophy,  Gliosarcoma,  Diabetic Foot Ulcers Deafness, Digenic, Gjb2/gjb3 Show all 22
GJA3 gap junction protein, alpha 3, 46kDa 13q12.11 Cataract 14, Multiple Types,  Zonular Pulverulent Cataract 3,  Cataract,  Cataract 4, Multiple Types,  Cataract 1, Multiple Types,  Cataract 6, Multiple Types,  Cataract 2, Multiple Types,  Posterior Polar Cataract Peripheral Neuropathy Show all 9
GJA4 gap junction protein, alpha 4, 37kDa 1p34.3 Myocardial Infarction,  Erythrokeratodermia Variabilis,  Atherosclerosis Peripheral Neuropathy Show all 4
GJA5 gap junction protein, alpha 5, 40kDa 1q21.2 Atrial Fibrillation, Familial, 11,  Atrial Standstill, Digenic,  Gja5-Related Familial Atrial Fibrillation,  Atrial Fibrillation, Familial, 3,  Familial Atrial Fibrillation,  Tetralogy Of Fallot,  Dilated Cardiomyopathy,  Peripheral Neuropathy Familial Dilated Cardiomyopathy Show all 9
GJA8 gap junction protein, alpha 8, 50kDa 1q21.2 Cataract 1, Multiple Types,  Cataract Microcornea Syndrome,  Zonular Pulverulent Cataract 1,  Cataracts, Autosomal Dominant,  Cataract 4, Multiple Types,  Cataract Peripheral Neuropathy Show all 7
GJB1 gap junction protein, beta 1, 32kDa Xq13.1 Charcot-Marie-Tooth Neuropathy X Type 1,  Inherited Peripheral Neuropathy,  Neuropathy,  Charcot-Marie-Tooth Neuropathy, X-Linked Dominant, 1,  Hypertrophic Neuropathy Of Dejerine-Sottas,  Charcot-Marie-Tooth Disease X-Linked 1,  Peripheral Neuropathy,  Sensory Neuropathy Type 1,  Charcot-Marie-Tooth Disease,  Charcot-Marie-Tooth Disease Type X,  X-Linked Disease,  Charcot-Marie-Tooth Neuropathy X,  Charcot-Marie-Tooth Neuropathy Type 2,  Charcot-Marie-Tooth Disease Type 1,  Charcot-Marie-Tooth Disease Type 4,  Hereditary Ataxia,  Hereditary Neuropathy With Liability To Pressure Palsies,  Charcot-Marie-Tooth Disease Type 2,  Spinocerebellar Ataxia, X-Linked 1,  Tooth Disease Charcot-Marie-Tooth Disease Type 3 Show all 21
GJB2 gap junction protein, beta 2, 26kDa 13q12.11 Bart-Pumphrey Syndrome,  Hypotrichosis-Deafness Syndrome,  Vohwinkel Syndrome,  Kid Syndrome,  Dfnb1,  Congenital Cytomegalovirus,  Mutism,  Deafness, Autosomal Dominant 3A,  Keratoderma Palmoplantar Deafness,  Gjb2-Related Dfna 3 Nonsyndromic Hearing Loss And Deafness,  Ichthyosis, Hystrix-Like, With Deafness,  Gjb2-Related Dfnb 1 Nonsyndromic Hearing Loss And Deafness,  Porokeratotic Eccrine Ostial And Dermal Duct Nevus,  Deafness, Autosomal Recessive 1A,  Cytomegalovirus Infection,  Nonsyndromic Hearing Loss And Deafness,  Keratitis,  Deafness And Hereditary Hearing Loss,  Deafness, Autosomal Dominant 3B,  Corneal Disease,  Deafness, Digenic, Gjb2/gjb3,  Dfna 3 Nonsyndromic Hearing Loss And Deafness,  Dfnb 1 Nonsyndromic Hearing Loss And Deafness,  Enlarged Vestibular Aqueduct,  Pendred Syndrome,  Clouston Syndrome,  Erythrokeratodermia Variabilis,  Keratoderma,  Auditory Neuropathy,  Nonsyndromic Hearing Loss And Deafness, Dfna3,  Focal Palmoplantar Keratoderma,  Sensorineural Hearing Loss,  Deafness, Digenic Gjb2/gjb6,  Pseudoainhum Nonsyndromic Hearing Loss And Deafness, Dfnb1 Show all 35
GJB3 gap junction protein, beta 3, 31kDa 1p34.3 Erythrokeratodermia Variabilis,  Nonsyndromic Hearing Loss And Deafness, Dfnb1,  Deafness, Digenic, Gjb2/gjb3,  Autosomal Recessive Nonsyndromic Deafness,  Deafness, Autosomal Dominant, With Peripheral Neuropathy,  Deafness, Autosomal Dominant 2B,  Neuropathy With Hearing Impairment,  Dfna 2B Nonsyndromic Hearing Loss And Deafness,  Gjb3-Related Erythrokeratodermia Variabilis,  Erythrokeratodermia Variabilis Et Progressiva,  Deafness, Autosomal Dominant 3B,  Peripheral Neuropathy,  Pseudoainhum,  Nonsyndromic Hearing Loss And Deafness,  Clouston Syndrome,  Enlarged Vestibular Aqueduct,  Dfnb1,  Hypotrichosis-Deafness Syndrome,  Keratoderma Palmoplantaris Transgrediens,  Skin Disease,  Kid Syndrome,  Sensorineural Hearing Loss,  Deafness And Hereditary Hearing Loss Nonsyndromic Deafness Show all 24
GJB4 gap junction protein, beta 4, 30.3kDa 1p34.3 Pseudoainhum,  Keratoderma Palmoplantaris Transgrediens,  Gjb4-Related Erythrokeratodermia Variabilis,  Erythrokeratodermia Variabilis,  Clouston Syndrome,  Hypotrichosis-Deafness Syndrome,  Erythrokeratodermia Variabilis Et Progressiva,  Kid Syndrome,  Peripheral Neuropathy Skin Disease Show all 10
GJB5 gap junction protein, beta 5, 31.1kDa 1p34.3 Lung Cancer Erythrokeratodermia Variabilis
GJB6 gap junction protein, beta 6, 30kDa 13q12.11 Hidrotic Ectodermal Dysplasia 2,  Dfna 3 Nonsyndromic Hearing Loss And Deafness,  Dfnb 1 Nonsyndromic Hearing Loss And Deafness,  Clouston Syndrome,  Nonsyndromic Hearing Loss And Deafness,  Nonsyndromic Hearing Loss And Deafness, Dfna3,  Deafness, Autosomal Dominant 3B,  Deafness, Digenic Gjb2/gjb6,  Gjb6-Related Dfna 3 Nonsyndromic Hearing Loss And Deafness,  Gjb6-Related Dfnb 1 Nonsyndromic Hearing Loss And Deafness,  Deafness, Autosomal Recessive 1B,  Dfnb1,  Kid Syndrome,  Deafness, Digenic, Gjb2/gjb3,  Bart-Pumphrey Syndrome,  Congenital Cytomegalovirus,  Ectodermal Dysplasia,  Pachyonychia Congenita,  Nonsyndromic Hearing Loss And Deafness, Dfnb1,  Palmoplantar Keratosis,  Auditory Neuropathy,  Pseudoainhum,  Enlarged Vestibular Aqueduct,  Peripheral Neuropathy Sensorineural Hearing Loss Show all 25
GJC1 gap junction protein, gamma 1, 45kDa 17q21.31 Cystic Fibrosis
GJC2 gap junction protein, gamma 2, 47kDa 1q42.13 Spastic Paraplegia 44, Autosomal Recessive,  Spastic Paraplegia 44,  Leukodystrophy, Hypomyelinating, 2,  Pelizaeus-Merzbacher-Like Disease 1,  Hereditary Lymphedema Ic,  Gjc2-Related Disorders,  Pelizaeus-Merzbacher Disease,  Lymphedema, Hereditary, Ia,  Hallermann-Streiff Syndrome,  Peripheral Neuropathy,  Lymphedema Leukodystrophy Show all 12
GJC3 gap junction protein, gamma 3, 30.2kDa 7q22.1 Peripheral Neuropathy
GJD2 gap junction protein, delta 2, 36kDa 15q14 Refractive Error,  Peripheral Neuropathy,  Juvenile Myoclonic Epilepsy,  Tremor Essential Tremor Show all 5
GJE1 gap junction protein, epsilon 1, 23kDa 6q24.1 Peripheral Neuropathy
GK glycerol kinase Xp21.2 Hyperglycerolemia,  Glycerol Kinase Deficiency, Infantile Form,  Glycerol Kinase Deficiency, Juvenile Form,  Glycerol Kinase Deficiency, Adult Form,  X-Linked Adrenal Hypoplasia Congenita,  Complex Glycerol Kinase Deficiency,  Aland Island Eye Disease,  Dystrophinopathies,  Duchenne Muscular Dystrophy,  Acute Liver Failure,  Metaphyseal Dysplasia Eye Disease Show all 12
GK2 glycerol kinase 2 4q21.21 X-Linked Adrenal Hypoplasia Congenita Complex Glycerol Kinase Deficiency
GKN1 gastrokine 1 2p13.3 Gastric Cancer
GKN2 gastrokine 2 2p13.3 Gastric Cancer
GLA galactosidase, alpha Xq22.1 Cramp-Fasciculation Syndrome,  Classic Fabry Disease,  Fabry Disease,  Priapism,  Fabry Disease, Cardiac Variant,  Hypohidrosis,  Anhidrosis,  Aortic Atherosclerosis,  Sphingolipidosis,  Galactosialidosis,  Keutel Syndrome,  Gangliosidosis Gm1,  Schindler Disease,  Fucosidosis,  Angiokeratoma,  X-Linked Disease,  Gangliosidosis,  Tay-Sachs Disease,  Autonomic Dysfunction,  Danon Disease Factor Vii Deficiency Show all 21
GLB1 galactosidase, beta 1 3p22.3 Glb1-Related Disorders,  Gangliosidosis Gm1,  Gm1 Gangliosidosis Type 2,  Gm1 Gangliosidosis Type 3,  Gm1 Gangliosidosis Type 1,  Gangliosidosis,  Costello Syndrome,  Galactosialidosis,  Mucopolysaccharidosis Iv,  Krabbe Disease Lactose Intolerance Show all 11
GLB1L galactosidase, beta 1-like 2q35 Mucopolysaccharidoses,  Morquio Syndrome B Sly Syndrome
GLC1B glaucoma 1, open angle, B (adult-onset) 2cen-q13 Glaucoma 1B, Primary Open Angle, Adult Onset
GLC1C glaucoma 1, open angle, C 3q21-q24 Glaucoma 1C, Primary Open Angle
GLC1D glaucoma 1, open angle, D (adult-onset) 8q23 Glaucoma 1D, Primary Open Angle
GLC1F glaucoma 1, open angle, F (adult-onset) 7q35-q36 Glaucoma 1, Open Angle, F
GLC1H glaucoma 1, open angle, H (adult-onset) 2p16.3-p15 Glaucoma 1, Open Angle, H
GLC1I glaucoma 1, open angle, I 15q11-q13 Glaucoma 1, Open Angle, I
GLC1K glaucoma 1, open angle, K (juvenile-onset) 20p12 Glaucoma 1K, Primary Open Angle, Juvenile-Onset
GLC1M glaucoma 1, open angle, M (juvenile-onset) 5q Glaucoma 1, Open Angle, M
GLC1N glaucoma 1, open angle, N (juvenile-onset) 15q22-q24 Glaucoma 1, Open Angle, N
GLC1P glaucoma 1, open angle, P 12q14 Glaucoma 1, Open Angle, P
GLC3B glaucoma 3, primary infantile, B 1p36 Glaucoma 3 Primary Infantile B,  Buphthalmos Primary Congenital Glaucoma
GLC3C glaucoma 3, primary congenital, C 14q24.3-q31.1 Glaucoma 3, Primary Congenital, C Primary Congenital Glaucoma
GLCCI1 glucocorticoid induced transcript 1 7p21.3 Glucocorticoid Therapy, Response To
GLDC glycine dehydrogenase (decarboxylating) 9p24.1 Gldc-Related Glycine Encephalopathy,  D-Glycericacidemia,  Glycine Encephalopathy,  Neonatal Glycine Encephalopathy,  Infantile Glycine Encephalopathy,  Atypical Glycine Encephalopathy Early Myoclonic Encephalopathy Show all 7
GLE1 GLE1 RNA export mediator 9q34.11 Lethal Congenital Contracture Syndrome 1,  Lethal Arthrogryposis With Anterior Horn Cell Disease,  Anterior Horn Cell Disease Congenital Contractures Show all 4
GLI1 GLI family zinc finger 1 12q13.3 Necrobiosis Lipoidica,  Ameloblastoma,  Plexiform Neurofibroma,  Basal Cell Carcinoma,  Anal Canal Carcinoma,  Olfactory Neuroblastoma,  Granuloma Annulare,  Pancreatic Cancer,  Pallister-Hall Syndrome,  Chondroma,  Colorectal Cancer,  Embryonal Rhabdomyosarcoma,  Holoprosencephaly,  Neurofibroma,  Neuroblastoma Medulloblastoma Show all 16
GLI2 GLI family zinc finger 2 2q14.2 Holoprosencephaly-9,  Gli2-Related Holoprosencephaly,  Pallister-Hall Syndrome 2,  Greig Cephalopolysyndactyly Syndrome,  Pallister-Hall Syndrome,  Calcifying Epithelial Odontogenic Tumor,  Holoprosencephaly-3,  Septopreoptic Holoprosencephaly,  Midline Interhemispheric Variant Of Holoprosencephaly,  Alobar Holoprosencephaly,  Vacterl Association,  Lobar Holoprosencephaly,  Polydactyly,  Holoprosencephaly, Recurrent Infections, And Monocytosis,  Septo-Optic Dysplasia,  Single Median Maxillary Central Incisor,  Semilobar Holoprosencephaly,  Split Hand Holoprosencephaly Show all 19
GLI3 GLI family zinc finger 3 7p14.1 Greig Cephalopolysyndactyly Syndrome,  Postaxial Polydactyly Type A,  Polydactyly,  Pallister-Hall Syndrome,  Hypothalamic Hamartomas,  Gli3-Related Disorders,  Polydactyly Preaxial Type 4,  Hypothalamic Hamartomas, Somatic,  Postaxial Polydactyly Type B, Bilateral,  Polydactyly, Postaxial, Types A1 And B,  Postaxial Polydactyly Type A, Bilateral,  Polysyndactyly, Bilateral,  Postaxial Polydactyly Type B, Unilateral,  Polysyndactyly, Unilateral,  Postaxial Polydactyly Type A, Unilateral,  Acrocallosal Syndrome,  Synovial Chondromatosis,  Talipes Equinovarus,  Imperforate Anus,  Tracheoesophageal Fistula Mckusick-Kaufman Syndrome Show all 21
GLIDR glioblastoma down-regulated RNA 9q13 Glioblastoma
GLIPR1 GLI pathogenesis-related 1 12q21.2 Prostate Cancer Glioblastoma Multiforme
GLIS2 GLIS family zinc finger 2 16p13.3 Nephronophthisis 7,  Acute Megakaryoblastic Leukemia Without Down Syndrome,  Nephronophthisis 1, Juvenile,  Juvenile Nephronophthisis Kidney Disease Show all 5
GLIS3 GLIS family zinc finger 3 9p24.2 Diabetes Mellitus, Neonatal, With Congenital Hypothyroidism,  Congenital Hypothyroidism Hypothyroidism
GLM4 Glioma, familial, 1 15q23-q26.3 Glioma Susceptibility 4
GLM5 Glioma susceptibility 5 9p21.3 Glioma Susceptibility 5
GLM6 Glioma susceptibility 6 20q13.33 Glioma Susceptibility 6
GLM7 Glioma susceptibility 7 8q24.21 Glioma Susceptibility 7
GLM8 Glioma susceptibility 8 5p15.33 Glioma Susceptibility 8
GLMN glomulin, FKBP associated protein 1p22.1 Familial Glomangioma,  Glomangioma,  Glomuvenous Malformation,  Coats Disease Klippel-Trenaunay Syndrome Show all 5
GLO1 glyoxalase I 6p21.2 Triosephosphate Isomerase Deficiency Tuberculosis
GLP1R glucagon-like peptide 1 receptor 6p21.2 Fasting Hypoglycemia,  Type 2 Diabetes Mellitus Obesity
GLRA1 glycine receptor, alpha 1 5q33.1 Sporadic Hyperekplexia,  Stiff-Person Syndrome,  Hyperekplexia,  Hyperekplexia, Hereditary 1, Autosomal Dominant Or Recessive,  Glra1-Related Hyperekplexia,  Aspiration Pneumonia Molybdenum Cofactor Deficiency Show all 7
GLRA2 glycine receptor, alpha 2 Xp22.2 Dyscalculia Hyperekplexia
GLRA3 glycine receptor, alpha 3 4q34.1 Hyperekplexia
GLRA4 glycine receptor, alpha 4 Xq22.2 Hyperekplexia
GLRB glycine receptor, beta 4q32.1 Glrb-Related Hyperekplexia,  Hyperekplexia 2, Autosomal Recessive,  Stiff-Person Syndrome,  Hyperekplexia,  Esotropia,  Hyperekplexia, Hereditary 1, Autosomal Dominant Or Recessive Glycine Encephalopathy Show all 7
GLRX glutaredoxin (thioltransferase) 5q15 Pancreatic Cystadenocarcinoma,  Transitional Meningioma Pancreatic Cancer
GLRX3 glutaredoxin 3 10q26.3 Lymphocytic Choriomeningitis
GLRX5 glutaredoxin 5 14q32.13 Pearson Syndrome,  Spasticity-Ataxia-Gait Anomalies Syndrome,  Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia Sideroblastic Anemia Show all 4
GLS glutaminase 2q32.2 Hepatic Encephalopathy,  Schizophrenia Paranoid Schizophrenia
GLS2 glutaminase 2 (liver, mitochondrial) 12q13.3 Stomach Carcinoma In Situ,  L-2-Hydroxyglutaric Aciduria,  2-Hydroxyglutaric Aciduria Schizophrenia Show all 4
GLTSCR2 glioma tumor suppressor candidate region gene 2 19q13.33 Seborrheic Keratosis
GLUD1 glutamate dehydrogenase 1 10q23.2 Hyperinsulinism-Hyperammonemia Syndrome,  Hyperinsulinism,  Glud1-Related Hyperinsulinism,  Spinocerebellar Degeneration,  Drug-Induced Hepatitis,  Lead Poisoning,  Fasting Hypoglycemia,  Olivopontocerebellar Atrophy,  Endometritis,  Leucine-Sensitive Hypoglycemia Of Infancy,  3-Hydroxyacyl-Coa Dehydrogenase Deficiency,  Familial Hyperinsulinism,  Canavan Disease,  Schizophrenia,  Acute Insulin Response Malaria Show all 16
GLUD1P5 glutamate dehydrogenase 1 pseudogene 5 10p11.2 Hyperinsulinism-Hyperammonemia Syndrome
GLUD2 glutamate dehydrogenase 2 Xq24 Parkinsons Disease Parkinson Disease, Late-Onset
GLUL glutamate-ammonia ligase 1q25.3 Glutamine Deficiency, Congenital,  Reye Syndrome,  Glutathione Synthetase Deficiency,  Retinal Detachment,  Acute Porphyria,  Schizophrenia,  Brain Edema Hepatic Encephalopathy Show all 8
GLYAT glycine-N-acyltransferase 11q12.1 Substance-Induced Psychosis,  Osteogenesis Imperfecta Type I Bullous Pemphigoid
GLYATL1 glycine-N-acyltransferase-like 1 11q12.1 Bacterial Conjunctivitis,  Acute Conjunctivitis Body Dysmorphic Disorder
GLYATL1P2 glycine-N-acyltransferase-like 1 pseudogene 2 11q12.1 Pulmonary Function
GLYCAM1 glycosylation dependent cell adhesion molecule 1 (pseudogene) 12q13.2 Macular Corneal Dystrophy
GLYCTK glycerate kinase 3p21.1 D-Glyceric Aciduria
GLYR1 glyoxylate reductase 1 homolog (Arabidopsis) 16p13.3 Band Keratopathy
GLYS1 glycosuria 1, renal 6p21.3 Renal Glycosuria
GM2A GM2 ganglioside activator 5q33.1 Gangliosidosis Gm2,  Gm2 Activator Deficiency,  Gm2-Gangliosidosis, Ab Variant,  Tay-Sachs Disease,  Gangliosidosis,  Sandhoff Disease Gm2-Gangliosidosis, Several Forms Show all 7
GMDS GDP-mannose 4,6-dehydratase 6p25.3 Leukocyte Adhesion Deficiency
GMNN geminin, DNA replication inhibitor 6p22.3 Melanoacanthoma Breast Cancer
GMPPA GDP-mannose pyrophosphorylase A 2q35 Alacrima, Achalasia, And Mental Retardation Syndrome,  Achalasia Triple-A Syndrome
GMPPB GDP-mannose pyrophosphorylase B 3p21.31 Granulomatous Amebic Encephalitis,  Muscular Dystrophy-Dystroglycanopathy , Type B, 14,  Muscular Dystrophy-Dystroglycanopathy , Type A, 14,  Muscular Dystrophy-Dystroglycanopathy , Type C, 14,  Muscular Dystrophy-Dystroglycanopathy , Type B, 5,  Muscular Dystrophy-Dystroglycanopathy , Type A, 1 Muscular Dystrophy-Dystroglycanopathy Show all 7
GMPS guanine monphosphate synthase 3q25.31 Acute Myeloid Leukemia, Adult Acute Myeloid Leukemia
GNA11 guanine nucleotide binding protein (G protein), alpha 11 (Gq class) 19p13.3 Hypocalciuric Hypercalcemia, Type Ii,  Hypocalcemia, Autosomal Dominant 2,  Foramen Magnum Meningioma,  Hypercalcemia,  Hypocalcemia, Autosomal Dominant,  Hypocalciuric Hypercalcemia, Type I Hypoparathyroidism Familial Isolated Show all 7
GNA12 guanine nucleotide binding protein (G protein) alpha 12 7p22.2 Familial Hyperaldosteronism
GNA14 guanine nucleotide binding protein (G protein), alpha 14 9q21.2 Pertussis,  Chorea-Acanthocytosis Acanthocytosis
GNAI1 guanine nucleotide binding protein (G protein), alpha inhibiting activity polypeptide 1 7q21.11 Pertussis
GNAI2 guanine nucleotide binding protein (G protein), alpha inhibiting activity polypeptide 2 3p21.31 Acth-Secreting Pituitary Adenoma,  Olivopontocerebellar Atrophy,  Ventricular Tachycardia, Idiopathic,  Hemiplegic Migraine,  Functioning Pituitary Adenoma,  Familial Hemiplegic Migraine Familial Hemiplegic Migraine Type 1 Show all 7
GNAI3 guanine nucleotide binding protein (G protein), alpha inhibiting activity polypeptide 3 1p13.3 Auriculocondylar Syndrome 1 Ankylosis
GNAL guanine nucleotide binding protein (G protein), alpha activating activity polypeptide, olfactory type 18p11.21 Dystonia 25,  Bipolar Disorder,  Schizophrenia,  Torsion Dystonia,  Blepharospasm Dystonia Show all 6
GNAO1 guanine nucleotide binding protein (G protein), alpha activating activity polypeptide O 16q12.2 Epileptic Encephalopathy, Early Infantile, 17 Epileptic Encephalopathy, Early Infantile, 2
GNAQ guanine nucleotide binding protein (G protein), q polypeptide 9q21.2 Sturge-Weber Syndrome,  Weber Syndrome,  Acanthocytosis,  Capillary Malformations, Congenital, 1, Somatic, Mosaic,  Sturge-Weber Syndrome, Somatic, Mosaic Chorea-Acanthocytosis Show all 6
GNAS GNAS complex locus 20q13.32 Progressive Osseous Heteroplasia,  Gnas Hyperfunction,  Monostotic Fibrous Dysplasia,  Sagliker Syndrome,  Mazabraud Syndrome,  Pseudopseudohypoparathyroidism,  Pseudohypoparathyroidism Type 1B,  Pseudohypoparathyroidism,  Acth-Independent Macronodular Adrenal Hyperplasia,  Fibrous Dysplasia,  Mccune Albright Syndrome,  Albrights Hereditary Osteodystrophy,  Pituitary Tumors,  Pseudohypoparathyroidism Type 1C,  Osseus Heteroplasia, Progressive,  Acromegaly, Somatic,  Mccune-Albright Syndrome, Somatic, Mosaic,  Acromegaly,  Somatostatin Analog,  Osteofibrous Dysplasia,  Acth-Secreting Pituitary Adenoma,  Growth Hormone Secreting Pituitary Adenoma,  Acrodysostosis,  Multinodular Goiter,  Villous Adenoma,  Ossifying Fibroma,  Osteitis Fibrosa,  Pituitary Adenoma,  Cherubism,  Primary Pigmented Nodular Adrenocortical Disease,  Goiter,  Ollier Disease,  Aip-Related Familial Isolated Pituitary Adenomas,  Familial Isolated Pituitary Adenoma,  Adenoma,  Multiple Endocrine Neoplasia,  Odontogenic Myxoma Myxofibrosarcoma Show all 38
GNAS-AS1 GNAS antisense RNA 1 20q13.32 Pseudohypoparathyroidism Pseudohypoparathyroidism Type 1B
GNAT1 guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 1 3p21.31 Autosomal Recessive Congenital Stationary Night Blindness,  Autosomal Dominant Congenital Stationary Night Blindness,  Congenital Stationary Night Blindness, Autosomal Dominant 3,  Fundus Albipunctatus,  Congenital Stationary Night Blindness,  Blindness,  Night Blindness,  Congenital Stationary Night Blindness, Autosomal Dominant 2 Retinal Disease Show all 9
GNAT2 guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 2 1p13.3 Achromatopsia 4,  Oligocone Trichromacy,  Congenital Nystagmus,  Achromatopsia,  Blue Cone Monochromacy,  Stargardt Disease Achromatopsia 2 Show all 7
GNAZ guanine nucleotide binding protein (G protein), alpha z polypeptide 22q11.22 Pertussis,  Autosomal Dominant Congenital Stationary Night Blindness Achromatopsia
GNB1 guanine nucleotide binding protein (G protein), beta polypeptide 1 1p36.33 Hemiplegic Migraine Familial Hemiplegic Migraine
GNB1L guanine nucleotide binding protein (G protein), beta polypeptide 1-like 22q11.21 Hypopharynx Cancer Digeorge Syndrome
GNB2L1 guanine nucleotide binding protein (G protein), beta polypeptide 2-like 1 5q35.3 Lung Cancer Wells Syndrome
GNB3 guanine nucleotide binding protein (G protein), beta polypeptide 3 12p13.31 Essential Hypertension,  Aortic Coarctation,  Hypertension,  Obesity,  Seasonal Affective Disorder,  Irritable Bowel Syndrome Schizophrenia Show all 7
GNB4 guanine nucleotide binding protein (G protein), beta polypeptide 4 3q26.33 Charcot-Marie-Tooth Disease, Dominant Intermediate F
GNE glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase 9p13.3 Gne-Related Myopathy,  Sialuria,  Sialuria, French Type,  Inclusion Body Myositis,  Oculopharyngodistal Myopathy,  Pagets Disease Of Bone,  Muscular Dystrophy With Rimmed Vacuoles Myopathy Show all 8
GNG2 guanine nucleotide binding protein (G protein), gamma 2 14q22.1 Hemiplegic Migraine Familial Hemiplegic Migraine
GNG8 guanine nucleotide binding protein (G protein), gamma 8 19q13.32 Pertussis
GNGT2 guanine nucleotide binding protein (G protein), gamma transducing activity polypeptide 2 17q21.32 Cll/sll
GNL3 guanine nucleotide binding protein-like 3 (nucleolar) 3p21.1 Squamous Cell Carcinoma Of The Head And Neck
GNLY granulysin 2p11.2 Tuberculosis,  Primary Biliary Cirrhosis,  Measles Folliculitis Show all 4
GNMT glycine N-methyltransferase 6p21.1 Glycine N-Methyltransferase Deficiency,  Hypermethioninemia Liver Cancer
GNPAT glyceronephosphate O-acyltransferase 1q42.2 Rhizomelic Chondrodysplasia Punctata Type 2,  Peroxisomal Disease,  Rhizomelic Chondrodysplasia Punctata,  Infantile Refsum Disease,  Chondrodysplasia,  Rhizomelic Chondrodysplasia Punctata Type 1,  Child Syndrome Refsum Disease Show all 8
GNPATP glyceronephosphate O-acyltransferase pseudogene 16q21 Pulmonary Function
GNPDA2 glucosamine-6-phosphate deaminase 2 4p12 Obesity
GNPTAB N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits 12q23.2 Mucolipidosis Iii Alpha/beta,  Mucolipidoses,  Mucolipidosis Ii,  Gnptab-Related Mucolipidoses,  Mucolipidosis,  Speech Disorder,  Mucopolysaccharidisis Type Iiia,  Mucolipidosis Iii Gamma Mucopolysaccharidosis Type Iiid Show all 9
GNPTG N-acetylglucosamine-1-phosphate transferase, gamma subunit 16p13.3 Mucolipidosis Iii Gamma,  Mucolipidosis Ii,  Speech Disorder,  Mucolipidosis Mucolipidosis Iii Alpha/beta Show all 5
GNRH1 gonadotropin-releasing hormone 1 (luteinizing-releasing hormone) 8p21.2 Hypogonadotropic Hypogonadism 12 With Or Without Anosmia,  Secondary Central Precocious Puberty,  Orbital Leiomyoma,  Penile Disease,  Catamenial Pneumothorax,  Sexual Disorder,  Pituitary Apoplexy,  Gnrh1-Related Isolated Gonadotropin-Releasing Hormone Deficiency,  Endometriosis,  Varicocele,  Central Precocious Puberty,  Ovarian Disease,  Anovulation,  Hypogonadotropic Hypogonadism 14 With Or Without Anosmia,  Ovarian Hyperstimulation Syndrome,  Endogenous Depression,  Isolated Gonadotropin-Releasing Hormone Deficiency,  Hypothalamic Hamartomas,  Myoma,  Leiomyoma,  Amenorrhea,  Aromatase Deficiency,  Myelomeningocele,  Priapism,  Robinow Syndrome,  Mccune Albright Syndrome,  Pituitary Adenoma,  Hypogonadism,  Idiopathic Central Precocious Puberty,  Polycystic Ovary Syndrome,  Prostate Cancer,  Maternal Uniparental Disomy, Chromosome 14,  Arachnoid Cysts,  Martsolf Syndrome,  Acth-Independent Macronodular Adrenal Hyperplasia,  Hypogonadotropism,  Cryptorchidism Endometrial Carcinoma Show all 38
GNRH2 gonadotropin-releasing hormone 2 20p13 Ovarian Cancer Medulloblastoma
GNRHR gonadotropin-releasing hormone receptor 4q13.2 Fertile Eunuch Syndrome,  Klinefelters Syndrome,  Hypogonadotropic Hypogonadism 7 Without Anosmia,  Gnrhr-Related Isolated Gonadotropin-Releasing Hormone Deficiency,  Hypogonadism,  Myoma,  Hypogonadotropic Hypogonadism 14 With Or Without Anosmia,  Oligospermia,  Ovarian Epithelial Cancer,  Endometrial Carcinoma Prostate Cancer Show all 11
GNS glucosamine (N-acetyl)-6-sulfatase 12q14.3 Mucopolysaccharidosis Type Iiid Mucopolysaccharidosis
GOLGA2 golgin A2 9q34.11 Mucopolysaccharidosis Iii
GOLGA5 golgin A5 14q32.12 Papillary Thyroid Carcinoma,  Oculocerebrorenal Syndrome Follicular Thyroid Carcinoma
GOLGA6A golgin A6 family, member A 15q24.1 Phobic Disorder,  Congenital Fibrosarcoma Fibrosarcoma
GOLGA6B golgin A6 family, member B 15q24.1 Phobic Disorder,  Congenital Fibrosarcoma Fibrosarcoma
GOLGA6L2 golgin A6 family-like 2 15q11.2 Speech Disorder
GOLIM4 golgi integral membrane protein 4 3q26.2 Nasopharynx Carcinoma
GOLM1 golgi membrane protein 1 9q21.33 Dyggve-Melchior-Clausen Syndrome
GOLPH3 golgi phosphoprotein 3 (coat-protein) 5p13.3 Specific Phobia Focal Dermal Hypoplasia
GOPC golgi-associated PDZ and coiled-coil motif containing 6q22.1 Globozoospermia,  Glioblastoma Cystic Fibrosis
GORAB golgin, RAB6-interacting 1q24.2 Geroderma Osteodysplastica Hypercementosis
GORASP2 golgi reassembly stacking protein 2, 55kDa 2q31.1 Exudative Vitreoretinopathy
GOSR2 golgi SNAP receptor complex member 2 17q21.32 Progressive Myoclonic Epilepsy 6,  Essential Hypertension,  Hypertension,  Myoclonus Epilepsy Progressive Myoclonus Epilepsy Show all 5
GOT1 glutamic-oxaloacetic transaminase 1, soluble 10q24.2 Aspartate Aminotransferase, Serum Level Of, Qtl1,  Exanthem,  Gallbladder Disease,  Reye Syndrome Acute Pyelonephritis Show all 5
GOT1L1 glutamic-oxaloacetic transaminase 1-like 1 8p11.23 Euthyroid Sick Syndrome
GOT2 glutamic-oxaloacetic transaminase 2, mitochondrial 16q21 Fascioliasis,  Gallbladder Disease,  Reye Syndrome Exanthem Show all 4
GP1BA glycoprotein Ib (platelet), alpha polypeptide 17p13.2 Pseudo-Von Willebrand Disease,  Type 2B Von Willebrand Disease,  Anterior Ischemic Optic Neuropathy,  Ischemic Optic Neuropathy,  Non-Arteritic Anterior Ischemic Optic Neuropathy,  Bernard-Soulier Syndrome Type A,  Bernard-Soulier Syndrome, Type A2,  Bernard-Soulier Syndrome, Type A1,  Von Willebrands Disease,  Bernard-Soulier Syndrome,  Infective Endocarditis,  Glanzmanns Thrombasthenia,  Thrombasthenia,  Endocarditis,  Giant Platelet Disorder, Isolated,  Bernard-Soulier Syndrome Type C,  Bernard-Soulier Syndrome Type B,  Coronary Thrombosis,  Thrombocytosis,  Fetal And Neonatal Alloimmune Thrombocytopenia,  Heparin-Induced Thrombocytopenia Thrombocytopenia Show all 22
GP1BB glycoprotein Ib (platelet), beta polypeptide 22q11.21 Giant Platelet Disorder, Isolated,  Bernard-Soulier Syndrome Type B,  Bernard-Soulier Syndrome,  Digeorge Syndrome,  Bernard-Soulier Syndrome, Type A2,  Bernard-Soulier Syndrome, Type A1,  Velocardiofacial Syndrome,  Bernard-Soulier Syndrome Type C Fetal And Neonatal Alloimmune Thrombocytopenia Show all 9
GP2 glycoprotein 2 (zymogen granule membrane) 16p12.3 Vesiculitis,  Ebola Hemorrhagic Fever,  Lassa Fever,  Lymphocytic Choriomeningitis,  Swine Influenza,  Familial Juvenile Hyperuricaemic Nephropathy Hemorrhagic Fever Show all 7
GP5 glycoprotein V (platelet) 3q29 Cervix Uteri Carcinoma In Situ,  Gray Platelet Syndrome Bernard-Soulier Syndrome
GP6 glycoprotein VI (platelet) 19q13.42 Cervix Uteri Carcinoma In Situ,  Glycoprotein 1A Deficiency,  Bleeding Disorder, Platelet-Type, 11,  Gray Platelet Syndrome Coronary Thrombosis Show all 5
GP9 glycoprotein IX (platelet) 3q21.3 Bernard-Soulier Syndrome,  Bernard-Soulier Syndrome Type C,  Gray Platelet Syndrome,  Bernard-Soulier Syndrome, Type A2,  Bernard-Soulier Syndrome, Type A1,  Giant Platelet Disorder, Isolated Bernard-Soulier Syndrome Type B Show all 7
GPBAR1 G protein-coupled bile acid receptor 1 2q35 Sclerosing Cholangitis,  Primary Sclerosing Cholangitis,  Nephrogenic Diabetes Insipidus Ocular Albinism Show all 4
GPBP1 GC-rich promoter binding protein 1 5q11.2 Atherosclerosis
GPC1 glypican 1 2q37.3 Biliary Atresia
GPC2 glypican 2 7q22.1 Mucopolysaccharidoses,  Morquio Syndrome B Sly Syndrome
GPC3 glypican 3 Xq26.2 Simpson-Golabi-Behmel Syndrome Type 1,  Simpson-Golabi-Behmel Syndrome,  Wilms Tumor, Somatic,  Gpc3-Related Simpson-Golabi-Behmel Syndrome Type 1,  Wilms Tumor,  Sotos Syndrome,  Embryonal Sarcoma,  Placental Site Trophoblastic Tumor,  Carotid Artery Dissection,  Extragonadal Germ Cell Tumor,  Proteus Syndrome Wilms Tumor, Type 1 Show all 12
GPC4 glypican 4 Xq26.2 Gpc4-Related Simpson-Golabi-Behmel Syndrome Type 1,  Simpson-Golabi-Behmel Syndrome Type 1,  Postaxial Polydactyly Type A,  Simpson-Golabi-Behmel Syndrome,  Postaxial Polydactyly, Type A2 Anoxia Show all 6
GPC6 glypican 6 13q31.3 Omodysplasia 1 Body Dysmorphic Disorder
GPD1 glycerol-3-phosphate dehydrogenase 1 (soluble) 12q13.12 Hypertriglyceridemia, Transient Infantile Hypertriglyceridemia
GPD1L glycerol-3-phosphate dehydrogenase 1-like 3p22.3 Brugada Syndrome 2,  Right Bundle Branch Block,  Sudden Infant Death Syndrome,  Brugada Syndrome Brugada Syndrome 1 Show all 5
GPD2 glycerol-3-phosphate dehydrogenase 2 (mitochondrial) 2q24.1 Type 2 Diabetes Mellitus,  Insulin Resistance,  Diabetes Mellitus, Noninsulin-Dependent, 2,  Diabetes Mellitus, Noninsulin-Dependent, Late Onset,  Diabetes Mellitus, Type 2, Susceptiblity To,  Diabetes Mellitus, Noninsulin-Dependent, Association With,  Hypertension, Insulin Resistance-Related,  Methylmalonic Acidemia Diabetes Mellitus, Noninsulin-Dependent Show all 9
GPDS1 glaucoma-related pigment dispersion syndrome 1 7q35-q36 Pigment-Dispersion Syndrome
GPER1 G protein-coupled estrogen receptor 1 7p22.3 Breast Cancer,  Pain Disorder Ovarian Cancer
GPHA2 glycoprotein hormone alpha 2 11q13.1 Norrie Disease
GPHN gephyrin 14q23.3 Molybdenum Cofactor Deficiency C,  Geniculate Herpes Zoster,  Gphn-Related Hyperekplexia,  Hyperekplexia,  Molybdenum Cofactor Deficiency,  Acute Monoblastic Leukemia,  Herpes Zoster,  Stiff-Person Syndrome,  Molybdenum Cofactor Deficiency A Hyperekplexia, Hereditary 1, Autosomal Dominant Or Recessive Show all 10
GPI glucose-6-phosphate isomerase 19q13.11 Glucose Phosphate Isomerase Deficiency,  Glucosephosphate Isomerase Deficiency,  Congenital Nonspherocytic Hemolytic Anemia,  Hydrops Fetalis,  Enamel Erosion,  Hemolytic Anemia,  Dentine Erosion,  Root Caries Primary Hyperoxaluria Show all 9
GPIHBP1 glycosylphosphatidylinositol anchored high density lipoprotein binding protein 1 8q24.3 Hyperlipoproteinemia, Type 1D,  Familial Lipoprotein Lipase Deficiency,  Hyperlipoproteinemia Type V,  Type 2 Diabetes Mellitus Hyperlipoproteinemia, Type Ib Show all 5
GPM6B glycoprotein M6B Xp22.2 Pelizaeus-Merzbacher Disease
GPNMB glycoprotein (transmembrane) nmb 7p15.3 Iris Disease Melanoma
GPR112 G protein-coupled receptor 112 Xq26.3 Neuroendocrine Carcinoma
GPR125 G protein-coupled receptor 125 4p15.2 Bipolar Disorder Schizophrenia
GPR143 G protein-coupled receptor 143 Xp22.2 Ocular Albinism, X-Linked,  Ocular Albinism,  Albinism,  Congenital Nystagmus,  Congenital Nystagmus 6, X-Linked,  Ocular Albinism, Type I, Nettleship-Falls Type Strabismus Show all 7
GPR148 G protein-coupled receptor 148 2q21.1 Cicatricial Entropion Entropion
GPR15 G protein-coupled receptor 15 3q11.2 Osteosarcoma Hiv-1
GPR152 G protein-coupled receptor 152 11q13.2 Estrogen-Receptor Positive Breast Cancer
GPR17 G protein-coupled receptor 17 2q14.3 Suppression Amblyopia,  Amblyopia Spinal Cord Injury
GPR171 G protein-coupled receptor 171 3q25.1 Usher Syndrome Type 3
GPR179 G protein-coupled receptor 179 17q12 Congenital Stationary Night Blindness, Type 1E,  Night Blindness, Congenital Stationary , 1E, Autosomal Recessive,  Blindness,  Congenital Stationary Night Blindness, Autosomal Dominant 2 Night Blindness Show all 5
GPR182 G protein-coupled receptor 182 12q13.3 Sepsis Oligohydramnios
GPR35 G protein-coupled receptor 35 2q37.3 Primary Sclerosing Cholangitis
GPR37 G protein-coupled receptor 37 (endothelin receptor type B-like) 7q31.33 Parkinsons Disease
GPR45 G protein-coupled receptor 45 2q12.1 Breast And Colorectal Cancer
GPR50 G protein-coupled receptor 50 Xq28 Mood Disorder Autism Spectrum Disorder
GPR56 G protein-coupled receptor 56 16q21 Bilateral Frontoparietal Polymicrogyria,  Polymicrogyria,  Bilateral Perisylvian Polymicrogyria,  Lennox-Gastaut Syndrome,  Neuronal Migration Disorders Periventricular Nodular Heterotopia Show all 6
GPR68 G protein-coupled receptor 68 14q32.11 Ovarian Cancer
GPR75 G protein-coupled receptor 75 2p16.2 Age Related Macular Degeneration
GPR78 G protein-coupled receptor 78 4p16.1 Schizophrenia
GPR83 G protein-coupled receptor 83 11q21 Dissecting Aortic Aneurysm
GPR84 G protein-coupled receptor 84 12q13.13 Pertussis
GPR87 G protein-coupled receptor 87 3q25.1 Lung Squamous Cell Carcinoma,  Oral Squamous Cell Carcinoma Breast And Colorectal Cancer
GPR98 G protein-coupled receptor 98 5q14.3 Febrile Seizures, Familial, 4,  Usher Syndrome,  Usher Syndrome, Type 2C,  Febrile Seizures,  Usher Syndrome Type 2A,  Usher Syndrome Type Ii,  Audiogenic Seizures,  Usher Syndrome, Type 2C, Gpr98/pdzd7 Digenic Usher Syndrome Type 3A Show all 9
GPRASP2 G protein-coupled receptor associated sorting protein 2 Xq22.1 Autism Spectrum Disorder
GPSM2 G-protein signaling modulator 2 1p13.3 Chudley-Mccullough Syndrome,  Autosomal Recessive Nonsyndromic Deafness,  Nonsyndromic Deafness Deafness, Digenic, Gjb2/gjb3 Show all 4
GPT glutamic-pyruvate transaminase (alanine aminotransferase) 8q24.3 Hemorrhagic Shock And Encephalopathy Syndrome,  Paraquat Poisoning,  Tinea Unguium,  Typhus,  Bile Duct Disease,  Viral Hepatitis,  Fatty Liver Disease,  Hemorrhagic Fever,  Hepatitis A,  Hepatitis E,  Scrub Typhus,  Choledocholithiasis,  Liver Cirrhosis,  Opisthorchiasis,  Necrotizing Fasciitis,  Nonalcoholic Steatohepatitis,  Fulminant Viral Hepatitis,  Cholangitis,  Liver Disease,  Afferent Loop Syndrome,  Hepatitis D,  Euthyroid Sick Syndrome,  Lymphogranuloma Venereum,  Coronary Aneurysm,  Citrin Deficiency,  Extrahepatic Cholestasis,  Polyarteritis Nodosa,  Kawasaki Disease,  Intrahepatic Cholestasis,  Human Monocytic Ehrlichiosis,  Chickenpox,  Viral Pneumonia,  Insulin Resistance,  Siderosis,  Neonatal Intrahepatic Cholestasis Caused By Citrin Deficiency,  Cholecystitis,  Vitelliform Macular Dystrophy,  Hepatitis B,  Alcohol Abuse,  Multiple Chemical Sensitivity,  Cholestasis,  Obesity,  Crigler-Najjar Syndrome,  Drug-Induced Hepatitis,  Congenital Cytomegalovirus,  Neuroleptic Malignant Syndrome,  Hepatitic C Virus,  Cholelithiasis,  Canavan Disease,  Biliary Atresia,  Fasciitis,  Dysferlinopathy,  Type 2 Diabetes Mellitus,  Hepatitis C Virus,  Hepatitis C,  Hypercholesterolemia Pre-Eclampsia Show all 57
GPX1 glutathione peroxidase 1 3p21.31 Hemolytic Anemia Due To Glutathione Peroxidase Deficiency,  Keshan Disease,  Breast Cancer,  Oral Cavity Cancer Malaria Show all 5
GPX1P2 glutathione peroxidase pseudogene 2 21q21.3 Major Depressive Disorder
GPX2 glutathione peroxidase 2 (gastrointestinal) 14q23.3 Non-Hodgkin Lymphoma Lung Cancer
GPX3 glutathione peroxidase 3 (plasma) 5q33.1 Keshan Disease
GPX4 glutathione peroxidase 4 19p13.3 Spondylometaphyseal Dysplasia Sedaghatian Type,  Keshan Disease Toxic Encephalopathy
GPX5 glutathione peroxidase 5 (epididymal androgen-related protein) 6p22.1 Keshan Disease
GPX6 glutathione peroxidase 6 (olfactory) 6p22.1 Keshan Disease
GPX7 glutathione peroxidase 7 1p32.3 Goldenhar Syndrome
GPX8 glutathione peroxidase 8 (putative) 5q11.2 Keshan Disease
GRAMD3 GRAM domain containing 3 5q23.2 Hepatitis C Virus Hepatitis C
GRB10 growth factor receptor-bound protein 10 7p12.1 Silver-Russell Syndrome Albrights Hereditary Osteodystrophy
GRB2 growth factor receptor-bound protein 2 17q25.1 Hydrocele
GRD1 Graves disease, susceptiblity to, 1 14q31 Graves Disease 1 Graves Disease
GRD2 Graves disease, susceptibility to, 2 20q13.11 Graves Disease 2 Graves Disease
GRDX Graves disease, susceptibility to, X-linked Xp11 Graves Disease X-Linked Graves Disease
GREB1 growth regulation by estrogen in breast cancer 1 2p25.1 Breast Cancer
GREB1L growth regulation by estrogen in breast cancer-like 18q11.1 Breast Cancer
GREM1 gremlin 1, DAN family BMP antagonist 15q13.3 Pauci-Immune Glomerulonephritis,  Colorectal Adenoma,  Renal Hypoplasia,  Norrie Disease,  Asphyxiating Thoracic Dystrophy,  Idiopathic Interstitial Pneumonia,  Adenoma,  Hereditary Mixed Polyposis Syndrome 2 Proliferative Vitreoretinopathy Show all 9
GREM2 gremlin 2, DAN family BMP antagonist 1q43 Accommodative Esotropia,  Esotropia Norrie Disease
GRHL2 grainyhead-like 2 (Drosophila) 8q22.3 Deafness, Autosomal Dominant 28,  Ectodermal Dysplasia/short Stature Syndrome,  Dfna28 Nonsyndromic Hearing Loss And Deafness Deafness, Autosomal Dominant 3B Show all 4
GRHL3 grainyhead-like 3 (Drosophila) 1p36.11 Van Der Woude Syndrome 2 Van Der Woude Syndrome
GRHPR glyoxylate reductase/hydroxypyruvate reductase 9p13.2 Primary Hyperoxaluria Type 2 Primary Hyperoxaluria
GRIA1 glutamate receptor, ionotropic, AMPA 1 5q33.2 Limbic Encephalitis
GRIA2 glutamate receptor, ionotropic, AMPA 2 4q32.1 Status Epilepticus,  Fraser Syndrome,  Amyotrophic Lateral Sclerosis,  Schizophrenia Lateral Sclerosis Show all 5
GRIA3 glutamate receptor, ionotropic, AMPA 3 Xq25 Rasmussen Encephalitis,  X-Linked Intellectual Disability Due To Gria3 Anomalies,  Auditory Neuropathy Canavan Disease Show all 4
GRIA4 glutamate receptor, ionotropic, AMPA 4 11q22.3 Schizophrenia
GRID2 glutamate receptor, ionotropic, delta 2 4q22.1 Autosomal Recessive Congenital Cerebellar Ataxia Due To Grid2 Deficiency Spinocerebellar Ataxia Type 5
GRIK1 glutamate receptor, ionotropic, kainate 1 21q21.3 Depersonalization Disorder,  Monosomy 21,  Juvenile Absence Epilepsy Amnestic Disorder Show all 4
GRIK2 glutamate receptor, ionotropic, kainate 2 6q16.3 Mental Retardation, Autosomal Recessive 2,  Hemimegalencephaly Juvenile Absence Epilepsy
GRIK3 glutamate receptor, ionotropic, kainate 3 1p34.3 Schizophrenia
GRIK5 glutamate receptor, ionotropic, kainate 5 19q13.2 Schizophrenia
GRIN1 glutamate receptor, ionotropic, N-methyl D-aspartate 1 9q34.3 Mental Retardation, Autosomal Dominant 8,  Dysembryoplastic Neuroepithelial Tumor,  Morphine Dependence,  Amblyopia,  Mental Retardation, Autosomal Dominant 6,  Tendinopathy,  Schizophrenia,  Neuroblastoma,  Sudden Infant Death Syndrome Bipolar Disorder Show all 10
GRIN2A glutamate receptor, ionotropic, N-methyl D-aspartate 2A 16p13.2 Epilepsy, Focal, With Speech Disorder And With Or Without Mental Retardation,  Speech Disorder,  Epilepsy With Neurodevelopmental Defects Early-Onset Epileptic Encephalopathy And Intellectual Disability Due To Grin2A Mutation Show all 4
GRIN2B glutamate receptor, ionotropic, N-methyl D-aspartate 2B 12p13.1 Mental Retardation, Autosomal Dominant 6,  Myoclonic Astatic Epilepsy,  Limbic Encephalitis Epileptic Encephalopathy, Early Infantile, 2 Show all 4
GRIN2C glutamate receptor, ionotropic, N-methyl D-aspartate 2C 17q25.1 Toxic Encephalopathy Schizophrenia
GRIN3B glutamate receptor, ionotropic, N-methyl-D-aspartate 3B 19p13.3 Opioid Abuse
GRIP1 glutamate receptor interacting protein 1 12q14.3 Cryptophthalmos,  Grip1-Related Fraser Syndrome Fraser Syndrome
GRK1 G protein-coupled receptor kinase 1 13q34 Oguchi Disease 2,  Fundus Albipunctatus,  Oguchi Disease 1,  Blindness,  Retinitis Pigmentosa Congenital Stationary Night Blindness, Autosomal Dominant 2 Show all 6
GRK4 G protein-coupled receptor kinase 4 4p16.3 Hypertension,  Aortic Coarctation Essential Hypertension
GRK6 G protein-coupled receptor kinase 6 5q35.3 Whim Syndrome
GRM1 glutamate receptor, metabotropic 1 6q24.3 Disuse Amblyopia,  Chondromyxoid Fibroma,  Spinocerebellar Ataxia, Autosomal Recessive 13,  Amblyopia,  Schizophrenia,  Bipolar Disorder,  Hypothalamic Hamartomas,  Hypocalcemia, Autosomal Dominant Breast Cancer Show all 9
GRM2 glutamate receptor, metabotropic 2 3p21.2 Schizophrenia
GRM3 glutamate receptor, metabotropic 3 7q21.11 Schizophrenia
GRM5 glutamate receptor, metabotropic 5 11q14.3 Synucleinopathy Fragile X Syndrome
GRM6 glutamate receptor, metabotropic 6 5q35.3 Suppression Amblyopia,  Optic Nerve Disease,  Amblyopia,  Congenital Stationary Night Blindness, Type 1B,  Night Blindness, Congenital Stationary , 1B, Autosomal Recessive,  Congenital Stationary Night Blindness, Autosomal Dominant 2 Autosomal Recessive Congenital Stationary Night Blindness Show all 7
GRN granulin 17q21.31 Ceroid Lipofuscinosis, Neuronal, 11,  Amusia,  Grn-Related Frontotemporal Dementia,  Impulse Control Disorder,  Frontotemporal Lobar Degeneration With Ubiquitin-Positive Inclusions,  Semantic Dementia,  Primary Progressive Aphasia,  Progressive Non-Fluent Aphasia,  Logopenic Progressive Aphasia,  Frontotemporal Dementia, Ubiquitin-Positive,  Aphasia,  Adrenal Carcinoma,  Frontotemporal Dementia,  Ceroid Lipofuscinosis, Neuronal, 4, Parry Type,  Dementia, Familial, Nonspecific,  Perry Syndrome,  Dementia Neuronal Ceroid-Lipofuscinoses Show all 18
GRP gastrin-releasing peptide 18q21.32 Diffuse Pulmonary Fibrosis,  Pancreatic Cancer,  Prostate Cancer,  Lung Cancer,  Thyroid Medullary Carcinoma,  Pulmonary Fibrosis,  Zollinger-Ellison Syndrome,  Neuroaxonal Dystrophy,  Congenital Central Hypoventilation Syndrome,  Anencephaly Central Hypoventilation Syndrome Show all 11
GRPR gastrin-releasing peptide receptor Xp22.2 Lung Cancer,  Prostate Adenocarcinoma,  Ovarian Epithelial Cancer,  Prostate Cancer Squamous Cell Carcinoma Of The Head And Neck Show all 5
GRXCR1 glutaredoxin, cysteine rich 1 4p13 Deafness, Autosomal Recessive 25 Deafness, Digenic, Gjb2/gjb3
GRXCR2 glutaredoxin, cysteine rich 2 5q32 Deafness, Autosomal Recessive 101 Deafness, Digenic, Gjb2/gjb3
GS1-204I12.1 uncharacterized LOC101929093 1q25.3 Prostate Cancer
GS1-251I9.4 uncharacterized LOC100506365 8q21.3 Migraine
GS1-279B7.1 microtubule-associated protein 1 light chain 3 beta pseudogene 1q25.3 Prostate Cancer
GSAP gamma-secretase activating protein 7q11.23 Alzheimers Disease
GSC goosecoid homeobox 14q32.13 Short Stature, Auditory Canal Atresia, Mandibular Hypoplasia, Skeletal Abnormalities,  Microtia,  Auditory Neuropathy Cornelia De Lange Syndrome Show all 4
GSC2 goosecoid homeobox 2 22q11.21 Digeorge Syndrome
GSDMB gasdermin B 17q12 Primary Biliary Cirrhosis
GSDMC gasdermin C 8q24.21 Melanoma
GSG2 germ cell associated 2 (haspin) 17p13.2 Rhinotracheitis
GSK3A glycogen synthase kinase 3 alpha 19q13.2 Schizophrenia
GSK3B glycogen synthase kinase 3 beta 3q13.33 Alzheimers Disease,  Aneurysmal Bone Cysts,  Parkinsons Disease,  Waardenburg Syndrome Type 2 Leopard Syndrome Show all 5
GSM1 geniospasm 1 9q13-q21 Geniospasm
GSN gelsolin 9q33.2 Lattice Corneal Dystrophy Type Ii,  Familial Amyloidosis, Finnish Type,  Blepharochalasis,  Finnish Type Amyloidosis,  Amyloidosis,  Lattice Corneal Dystrophy,  Hereditary Amyloidosis,  Corneal Disease,  Colorectal Cancer Renal Clear Cell Carcinoma Show all 10
GSR glutathione reductase 8p12 Pyridoxine Deficiency,  Hemolytic Anemia Due To Glutathione Reductase Deficiency,  Riboflavin Deficiency,  Diabetic Cataract,  Trypanosomiasis,  Malaria,  Primary Hyperoxaluria,  Primary Hyperoxaluria Type 2,  Nodular Goiter,  Ariboflavinosis,  Rasmussen Encephalitis,  Methemoglobinemia,  Glucosephosphate Dehydrogenase Deficiency,  Hereditary Pancreatitis,  Limbic Encephalitis,  Tuberous Sclerosis,  Encephalitis,  Lipomatosis,  Senile Cataract,  Variegate Porphyria,  Chagas Disease Myocardial Infarction Show all 22
GSS glutathione synthetase 20q11.22 Hemolytic Anemia Due To Glutathione Synthetase Deficiency,  Glutathione Synthetase Deficiency,  Metabolic Acidosis Anoxia Show all 4
GSTA1 glutathione S-transferase alpha 1 6p12.2 Toxic Encephalopathy
GSTA2 glutathione S-transferase alpha 2 6p12.2 Toxic Encephalopathy,  Malignant Pleural Mesothelioma Periventricular Nodular Heterotopia
GSTA3 glutathione S-transferase alpha 3 6p12.2 Toxic Encephalopathy Juvenile Myoclonic Epilepsy
GSTA4 glutathione S-transferase alpha 4 6p12.2 Atherosclerosis Malignant Pleural Mesothelioma
GSTM1 glutathione S-transferase mu 1 1p13.3 Lung Cancer, Gstm1-Related,  Oral Cancer,  Lung Cancer,  Asbestosis,  Leukoplakia,  Esophageal Cancer,  Cardia Cancer,  Scabies,  Colorectal Cancer,  Drug-Induced Hepatitis,  Malaria,  Mutagen Sensitivity,  Exfoliation Syndrome,  Open-Angle Glaucoma,  Senile Cataract,  Hereditary Pancreatitis,  Benzene Toxicity,  Primary Open Angle Glaucoma,  Multiple Chemical Sensitivity,  Beta Thalassemia,  Diffuse Gastric Cancer,  Prostate Cancer,  Laryngeal Squamous Cell Carcinoma,  Breast Cancer,  Breast Cancer Susceptibility Bladder Cancer Susceptibility Show all 26
GSTM3 glutathione S-transferase mu 3 (brain) 1p13.3 Bronchogenic Carcinoma,  Laryngeal Squamous Cell Carcinoma,  Oral Cancer,  Oral Leukoplakia,  Malignant Pleural Mesothelioma,  Non-Hodgkin Lymphoma,  Hereditary Pancreatitis,  Kidney Cancer,  Lung Cancer,  Barretts Adenocarcinoma Breast Cancer Show all 11
GSTM4 glutathione S-transferase mu 4 1p13.3 Tinea Pedis Breast Cancer Susceptibility
GSTM5 glutathione S-transferase mu 5 1p13.3 Breast Cancer Susceptibility
GSTO1 glutathione S-transferase omega 1 10q25.1 Cisplatin Toxicity,  Parkinsons Disease,  Barretts Adenocarcinoma Vascular Dementia Show all 4
GSTO2 glutathione S-transferase omega 2 10q25.1 Barretts Adenocarcinoma Parkinsons Disease
GSTP1 glutathione S-transferase pi 1 11q13.2 Maxillary Sinus Squamous Cell Carcinoma,  Cardia Cancer,  Pre-Eclampsia,  Barretts Esophagus,  Lung Cancer,  Plasmodium Vivax Malaria,  Oral Cancer,  Exfoliation Syndrome,  Prostate Cancer,  Epstein-Barr Virus-Associated Gastric Carcinoma,  Breast Cancer,  Hereditary Pancreatitis,  Bladder Cancer Susceptibility,  Eclampsia,  Multiple Chemical Sensitivity Diffuse Gastric Cancer Show all 16
GSTT1 glutathione S-transferase theta 1 22q11.23 Asbestosis,  Oral Cancer,  Laryngeal Carcinoma,  Mutagen Sensitivity,  Cardia Cancer,  Exfoliation Syndrome,  Drug-Induced Hepatitis,  Senile Cataract,  Lung Cancer,  Laryngeal Squamous Cell Carcinoma,  Benzene Toxicity,  Oligospermia,  Hereditary Pancreatitis,  Leukoplakia,  Multiple Chemical Sensitivity,  Beta Thalassemia,  Diffuse Gastric Cancer,  Prostate Cancer,  Toxic Encephalopathy,  Rosacea,  Myelodysplastic Syndromes,  Oral Submucous Fibrosis,  Breast Cancer,  Cervical Cancer,  Colorectal Cancer Breast Cancer Susceptibility Show all 26
GSTT2 glutathione S-transferase theta 2 22q11.23 Barretts Adenocarcinoma,  Colon Adenoma Malignant Pleural Mesothelioma
GSTZ1 glutathione S-transferase zeta 1 14q24.3 Tyrosinemia, Type Ib,  Tyrosinemia Type I,  Alkaptonuria,  Tyrosinemia,  Phenylketonuria Barretts Adenocarcinoma Show all 6
GSX1 GS homeobox 1 13q12.2 Moebius Syndrome
GTF2E1 general transcription factor IIE, polypeptide 1, alpha 56kDa 3q13.33 Richters Syndrome
GTF2H1 general transcription factor IIH, polypeptide 1, 62kDa 11p15.1 Rift Valley Fever Xeroderma Pigmentosum, Group C
GTF2H2 general transcription factor IIH, polypeptide 2, 44kDa 5q13.2 Werdnig-Hoffmann Disease,  Idiopathic Pulmonary Fibrosis,  Muscular Atrophy Seminoma Show all 4
GTF2H4 general transcription factor IIH, polypeptide 4, 52kDa 6p21.33 Nonphotosensitive Trichothiodystrophy Photosensitive Trichothiodystrophy
GTF2H5 general transcription factor IIH, polypeptide 5 6q25.3 Trichothiodystrophy, Complementation Group A Photosensitive Trichothiodystrophy
GTF2I general transcription factor IIi 7q11.23 Williams-Beuren Syndrome
GTF2IRD1 GTF2I repeat domain containing 1 7q11.23 Williams-Beuren Syndrome Williams Syndrome
GTF2IRD2 GTF2I repeat domain containing 2 7q11.23 Williams-Beuren Syndrome
GTF2IRD2B GTF2I repeat domain containing 2B 7q11.23 Williams-Beuren Syndrome
GTF3A general transcription factor IIIA 13q12.2 Prostate Carcinoma In Situ Endocarditis
GTS Gilles de la Tourette syndrome 11q23 Gilles De La Tourette Syndrome
GUCA1A guanylate cyclase activator 1A (retina) 6p21.1 Cone-Rod Dystrophy 14,  Cone Dystrophy 3,  Cone Dystrophy,  Partial Central Choroid Dystrophy,  Blue Cone Monochromacy,  Cone-Rod Dystrophy 2 Cone-Rod Dystrophy Show all 7
GUCA1B guanylate cyclase activator 1B (retina) 6p21.1 Retinitis Pigmentosa 48,  Guca1B-Related Retinitis Pigmentosa Retinitis Pigmentosa
GUCA2A guanylate cyclase activator 2A (guanylin) 1p34.2 Cystic Fibrosis Cholera
GUCA2B guanylate cyclase activator 2B (uroguanylin) 1p34.2 Ovarian Mucinous Neoplasm,  Cystic Fibrosis,  Colorectal Cancer Pertussis Show all 4
GUCY1A2 guanylate cyclase 1, soluble, alpha 2 11q22.3 Colorectal Cancer
GUCY1A3 guanylate cyclase 1, soluble, alpha 3 4q32.1 Moyamoya 6 With Achalasia,  Myocardial Infarction,  Myocardial Infarction, Decreased,  Myocardial Infarcation Myocardial Infarction, Protection Against Show all 5
GUCY2C guanylate cyclase 2C (heat stable enterotoxin receptor) 12p12.3 Ileus,  Meconium Ileus,  Chronic Diarrhea Due To Guanylate Cyclase 2C Overactivity,  Ovarian Mucinous Neoplasm,  Diarrhea,  Intestinal Obstruction Colorectal Cancer Show all 7
GUCY2D guanylate cyclase 2D, membrane (retina-specific) 17p13.1 Cone-Rod Dystrophy 6,  Leber Congenital Amaurosis 1,  Gucy2D-Related Leber Congenital Amaurosis,  Aipl1-Related Leber Congenital Amaurosis,  Keratoconus,  Partial Central Choroid Dystrophy,  Rpe65-Related Leber Congenital Amaurosis,  Leber Congenital Amaurosis,  Hyperopia,  Cone-Rod Dystrophy,  Leber Congenital Amaurosis 10,  Cone-Rod Dystrophy 2,  Choriodal Dystrophy, Central Areolar 2 Retinitis Pigmentosa Show all 14
GUCY2F guanylate cyclase 2F, retinal Xq23 Retinitis Pigmentosa
GUK1 guanylate kinase 1 1q42.13 Ankylosis
GULOP gulonolactone (L-) oxidase, pseudogene 8p21.1 Scurvy
GUSB glucuronidase, beta 7q11.21 Necrotizing Ulcerative Gingivitis,  Non-Immune Hydrops Fetalis,  Immune Hydrops Fetalis,  Bronchopneumonia,  Gingivitis,  Sly Syndrome,  Choledocholithiasis,  Hydrops Fetalis,  Chediak-Higashi Syndrome,  Fascioliasis,  Acalculous Cholecystitis,  Cholelithiasis,  Viral Meningitis,  Cholecystitis,  Meningitis,  Fabry Disease,  Vacuolar Myopathy,  Mouth Disease,  Mucolipidoses,  Bacteremia,  Tuberculosis,  Infectious Mononucleosis,  Alveolar Soft Part Sarcoma,  Mucopolysaccharidosis Leukopenia Show all 25
GUST Gustavson mental retardation syndrome (with microcephaly, optic Xq26 X-Linked Mental Retardation Gustavson Type
GYG1 glycogenin 1 3q24 Glycogen Storage Disease Xv,  Ornithosis Lymphogranuloma Venereum
GYG2 glycogenin 2 Xp22.33 Glycogen Storage Disease Type 0
GYLTL1B glycosyltransferase-like 1B 11p11.2 Ureteral Benign Neoplasm Dyscalculia
GYPA glycophorin A (MNS blood group) 4q31.21 Malaria,  Autoimmune Hemolytic Anemia,  Werner Syndrome Cerebral Malaria Show all 4
GYPB glycophorin B (MNS blood group) 4q31.21 Malaria Cerebral Malaria
GYPC glycophorin C (Gerbich blood group) 2q14.3 Malaria,  Hereditary Elliptocytosis Herpes Zoster
GYPE glycophorin E (MNS blood group) 4q31.21 Congenital Dyserythropoietic Anemia Type I,  Malaria Sickle Cell Disease
GYS1 glycogen synthase 1 (muscle) 19q13.33 Glycogen Storage Disease Type 0, Muscle,  Glucose Intolerance,  Insulin Resistance Type 2 Diabetes Mellitus Show all 4
GYS2 glycogen synthase 2 (liver) 12p12.1 Glycogen Storage Disease Type 0,  Fasting Hypoglycemia Hypoglycemia
GZMA granzyme A (granzyme 1, cytotoxic T-lymphocyte-associated serine esterase 3) 5q11.2 Chediak-Higashi Syndrome
GZMB granzyme B (granzyme 2, cytotoxic T-lymphocyte-associated serine esterase 1) 14q12 Subcutaneous Panniculitis-Like T-Cell Lymphoma,  Peripheral T-Cell Lymphoma,  Alopecia Areata,  Rasmussen Encephalitis,  Keratoacanthoma,  Composite Lymphoma,  Panniculitis,  Exanthem,  Myocardial Infarction,  Toxic Epidermal Necrolysis,  Stevens-Johnson Syndrome,  Cowpox,  Anaplastic Large Cell Lymphoma,  Giardiasis,  Lymphomatoid Papulosis,  Alopecia Cervical Intraepithelial Neoplasia Show all 17
GZMK granzyme K (granzyme 3; tryptase II) 5q11.2 Arts Syndrome,  Allergic Asthma T-Cell Large Granular Lymphocyte Leukemia


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