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
5271 to 5280 of 15448 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

5271
Guanine monophosphate synthase
GATD7
Cataract, Insomnia

5272
G protein subunit alpha 11
FBH, FBH2, FHH2, GNA-11, HG1K, HHC2, HYPOC2
Anastomosing haemangioma, Hypocalcemia, Calcium metabolism disorders, Capillary malformation, Congenital venous anomaly, Congenital heart defects, Congenital hemangioma, Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi, Cutis marmorata telangiectatica congenita, Hypocalciuric hypercalcemia, Congenital heart defect, Melanoma, Schwartz-jampel syndrome, Uveal melanoma

5273
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)

5274
G protein subunit alpha 13
G13, HG1N
Burkitt lymphoma, Hypertension

5275
G protein subunit alpha 14
HG1I
Anastomosing haemangioma, Bipolar disorder, Cerebrofacial arteriovenous metameric syndrome, Liver cirrhosis, Scoliosis, Myopia

5276
G protein subunit alpha 15
GNA16, HG1L
Asthma, Cardiomyopathy, Heart failure, Myocarditis, Respiratory system disease

5277
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

5278
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

5279
G protein subunit alpha i3
87U6, ARCND1, ARCODS, HG1A
Amnesia, Auriculocondylar syndrome, Desbuquois syndrome, Gout, Major depressive disorder, Metabolic syndrome, Diabetes mellitus type 2

5280
G protein subunit alpha L
DYT25, HG1O
Focal dystonia, Bipolar disorder, Dysarthria, Dystonia, Dystonia musculorum deformans, Genetic torsion dystonia, Schizophrenia, Venous thromboembolism