Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "G"

331 to 340 of 677 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
331	2768	GNA12	G protein subunit alpha 12	HG1M1, NNX3, RMP, gep	Ankylosing spondylitis, Atrial fibrillation, Bipolar disorder, Ulcerative colitis, Obstructive pulmonary disease, Colorectal cancer, Congenital cardiovascular anomaly, Crohn disease, Dementia, Hypertension, Hypothyroidism, Inflammatory bowel disease, Insomnia, Major depressive disorder, Myocardial ischemia View all (10 more)
332	10672	GNA13	G protein subunit alpha 13	G13, HG1N	Burkitt lymphoma, Hypertension
333	9630	GNA14	G protein subunit alpha 14	HG1I	Anastomosing haemangioma, Bipolar disorder, Cerebrofacial arteriovenous metameric syndrome, Liver cirrhosis, Scoliosis, Myopia
334	2769	GNA15	G protein subunit alpha 15	GNA16, HG1L	Asthma, Cardiomyopathy, Heart failure, Myocarditis, Respiratory system disease
335	2770	GNAI1	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
336	2771	GNAI2	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, Liver cirrhosis, Long qt syndrome, Cushing's disease, Retractile testis, Substance abuse, Familial ventricular tachycardia
337	2773	GNAI3	G protein subunit alpha i3	87U6, ARCND1, ARCODS, HG1A	Amnesia, Auriculocondylar syndrome, Desbuquois syndrome, Gout, Major depressive disorder, Metabolic syndrome, Diabetes mellitus type 2
338	2774	GNAL	G protein subunit alpha L	DYT25, HG1O	Focal dystonia, Bipolar disorder, Dysarthria, Dystonia, Dystonia musculorum deformans, Genetic torsion dystonia, Schizophrenia, Venous thromboembolism
339	2775	GNAO1	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 View all (3 more)
340	2776	GNAQ	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)

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