Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All 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
5251 to 5260 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

5251
G protein subunit alpha 15
GNA16, HG1L
Asthma, Cardiomyopathy, Heart failure, Respiratory system disease

5252
G protein subunit alpha i1
Gi, HG1B, NEDHISB
Amnesia, Asthma, Neurodevelopmental disorder, Developmental disability, Essential tremor, Renal pelvis neoplasms, Non-specific syndromic intellectual disability, Schizophrenia, Substance abuse

5253
G protein subunit alpha i2
GIP, GNAI2B, HG1C, H_LUCA15.1, H_LUCA16.1
Atrioventricular block, Bradycardia, Breast neoplasms, Cannabis abuse, Carcinoma, Ventricular tachycardia, Hypopituitarism, Insomnia, Long qt syndrome, Cushing's disease, Retractile testis, Substance abuse, Familial ventricular tachycardia

5254
G protein subunit alpha i3
87U6, ARCND1, ARCODS, HG1A
Amnesia, Auriculocondylar syndrome, Desbuquois syndrome, Gout, Major depressive disorder, Metabolic syndrome, Diabetes mellitus type 2

5255
G protein subunit alpha L
DYT25, HG1O
Focal dystonia, Bipolar disorder, Dysarthria, Dystonia, Dystonia musculorum deformans, Genetic torsion dystonia, Schizophrenia, Venous thromboembolism

5256
G protein subunit alpha o1
DEE17, EIEE17, G-ALPHA-o, GNAO, HG1G, HLA-DQB1, NEDIM
Breast cancer, Hepatocellular carcinoma, Cardioembolic stroke, Chorea, Choreoathetosis, Congenital neurologic anomalies, Developmental and epileptic encephalopathy, Developmental delay, Dyskinesia, Epilepsy, Essential tremor, Insomnia, Major depressive disorder, Movement disorder, Neurodevelopmental disorder
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5257
G protein subunit alpha q
CMAL, CMC1, G-ALPHA-q, GAQ, SWS
Anastomosing haemangioma, Bipolar disorder, Blood coagulation disorder, Capillary malformation, Capillary malformation-arteriovenous malformation, Congenital heart defects, Congenital hemangioma, Congestive heart failure, Craniofacial abnormalities, Duodenal ulcer, Dyslexia, Focal glomerulosclerosis, Congenital heart defect, Heart failure, Klippel-trenaunay syndrome
View all (3 more)

5258
GNAS complex locus
AHO, AIMAH1, C20orf45, GNAS1, GPSA, GSA, GSP, NESP, PITA3, POH, SCG6, SgVI
Brachydactyly, Cafe-au-lait spots, Cholangiocarcinoma, Cholecystolithiasis, Colorectal cancer, Cushing syndrome, Primary bilateral macronodular adrenal hyperplasia, Desbuquois syndrome, Duane retraction syndrome, Duodenal ulcer, Endocrine system disease, Depression, Gallstones, Gastric ulcer, Gout
View all (18 more)

5259
G protein subunit alpha transducin 1
CSNB1G, CSNBAD3, GBT1, GNATR, HG1F
Cannabis abuse, Congenital stationary night blindness, Major depressive disorder, Insomnia, Night blindness, congenital stationary, Oguchi disease, Retinal degeneration, Retinitis pigmentosa, Schizophrenia, Diabetes mellitus type 2

5260
G protein subunit alpha transducin 2
ACHM4, GNATC, HG1D
Achromatopsia, Color vision deficiency, Cone dystrophy, Gout, Metabolic syndrome, Obesity, Retinitis pigmentosa, Diabetes mellitus type 2