Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "A"
271 to 280 of 912 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

271
Acyl-CoA synthetase long chain family member 4
ACS4, FACL4, LACS4, MRX63, MRX68, XLID63
Experimental arthritis, Autism, Hepatocellular carcinoma, Major depressive disorder, Global developmental delay, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Depression, X-linked intellectual disability, Prostatic neoplasm

272
Aldehyde dehydrogenase 1 family member B1
ALDH5, ALDHX
Central nervous system cancer, Cholelithiasis, Colonic neoplasm, Color vision deficiency, Neurodevelopmental disorder, Glioblastoma, Glioma, Hepatomegaly, Liver cirrhosis, Nonalcoholic fatty liver disease, Non-specific syndromic intellectual disability

273
APC membrane recruitment protein 2
FAM123A
Brain aneurysm, Pelvic organ prolapse

274
Armadillo repeat containing 3
CT81, KU-CT-1, VAC8
Scoliosis, Systemic lupus erythematosus

275
ATP binding cassette subfamily B member 7
ABC7, ASAT, Atm1p, EST140535
Sideroblastic anemia, Ataxia, Mitochondrial disease, Spinocerebellar ataxia, x-linked, X-linked sideroblastic anemia

276
Aldehyde dehydrogenase 1 family member A3
ALDH1A6, ALDH6, MCOP8, RALDH3
Autism, Colobomatous microphthalmia, Melanoma, Microphthalmia, Microphthalmos, Nanophthalmos, Stomach neoplasms

277
Atonal bHLH transcription factor 7
Math5, NCRNA, PHPVAR, RNANC, bHLHa13
Alzheimer disease, Anterior segment dysgenesis, Congenital cataract microcornea with corneal opacity, Open angle glaucoma

278
Aldehyde dehydrogenase 3 family member B1
ALDH4, ALDH7
Autism, Schizophrenia

279
ARF like GTPase 5B
ARL8
Atrial fibrillation, Henoch schoenlein purpura, Melanoma, Venous thromboembolism

280
Adenylate kinase 9
AK 9, AKD1, AKD2, C6orf199, C6orf224, SPGF89, dJ70A9.1
Atrial fibrillation, Hepatitis b virus infection, Clonal hematopoiesis, Lung cancer, Major depressive disorder, Postsynaptic congenital myasthenic syndrome, Scoliosis, Spermatogenic failure