Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "G"

341 to 350 of 677 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
341	2778	GNAS	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)
342	2779	GNAT1	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
343	2780	GNAT2	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
344	346562	GNAT3	G protein subunit alpha transducin 3	GDCA, HG1E	Male infertility
345	2781	GNAZ	G protein subunit alpha z	HG1H, gz-alpha	Hepatocellular carcinoma
346	2782	GNB1	G protein subunit beta 1	HG2A, MDS, MRD42	Anxiety disorder, Autism, Nonsyndromic intellectual disability, Cerebral palsy, Congestive heart failure, Major depressive disorder, Developmental regression, Focal onset epileptic seizure, Global developmental delay, Heart failure, Hypothyroidism, Intellectual developmental disorder, Lymphoblastic leukemia, Myelodysplastic syndrome, Neurodevelopmental disorder View all (3 more)
347	54584	GNB1L	G protein subunit beta 1 like	DGCRK3, FKSG1, GY2, WDR14, WDVCF	Bipolar disorder, Glaucoma, Non-organic psychosis, Open angle glaucoma, Psychotic disorders, Schizophrenia
348	2783	GNB2	G protein subunit beta 2	HG2C1, NEDHYDF, SSS4, SSS4; NEDHYDF	Alzheimer disease, Sick sinus syndrome, Global developmental delay, Neurodevelopmental disorder, Non-specific syndromic intellectual disability
349	2784	GNB3	G protein subunit beta 3	CSNB1H, HG2D	Bipolar disorder, Carotid artery disease, Ischemic heart disease, Congenital stationary night blindness, Coronary artery disease, Major depressive disorder, Diabetes mellitus type 2, Hypertension, Eye disease, Hyperlipidemia, Hyperlipoproteinemia, Mood disorder, Myocardial ischemia, Night blindness, congenital stationary, Obesity View all (6 more)
350	59345	GNB4	G protein subunit beta 4	CMTD1F, HG2B	Atrial fibrillation, Charcot-marie-tooth disease, Colorectal neoplasms, Dejerine-sottas disease, Hereditary motor and sensory neuropathies, Hypertrophic neuropathy, Peroneal muscle atrophy, Roussy-levy syndrome

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