Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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5261 to 5270 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

5261
G protein subunit alpha transducin 3
GDCA, HG1E
Male infertility

5262
G protein subunit alpha z
HG1H, gz-alpha
Hepatocellular carcinoma

5263
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)

5264
G protein subunit beta 1 like
DGCRK3, FKSG1, GY2, WDR14, WDVCF
Bipolar disorder, Glaucoma, Non-organic psychosis, Open angle glaucoma, Psychotic disorders, Schizophrenia

5265
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

5266
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)

5267
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

5268
G protein subunit beta 5
GB5, HG2E, IDDCA, LADCI, LDMLS1, LDMLS2, gbeta5
Attention deficit hyperactivity disorder, Breast cancer, Colorectal neoplasms, Congenital neurologic anomalies, Fraser syndrome, Global developmental delay, Schizophrenia, Uveal melanoma

5269
Glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase
DMRV, GLCNE, IBM2, NM, THC12, Uae1
Atypical femoral fracture, Platelet-type bleeding disorder, Color vision deficiency, Congenital myopathy, Distal myopathy, Generalized anxiety disorder, Myositis, Thrombocytopenia, Vacuolar myopathy

5270
G protein subunit gamma 11
GNGT11, HG3H1
Juvenile arthritis, Central nervous system cancer, Color vision deficiency, Glioblastoma, Glioma, Juvenile idiopathic arthritis, Oligoarticular juvenile idiopathic arthritis