Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "A"
351 to 360 of 912 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

351
Ataxin 10
ATX10, E46L, HUMEEP, SCA10
Alzheimer disease, Breast cancer, Color vision deficiency, Laryngeal carcinoma, Laryngeal cancer, Scoliosis, Spinocerebellar ataxia, Diabetes mellitus, type 2, Ulcerative colitis

352
Ankyrin repeat and BTB domain containing 2
ABTB2A, BTBD22, CCA3
Brain infarction, Cerebral amyloid angiopathy, Color vision deficiency, Insomnia, Lewy body disease, Ocular hypotension, Severe acute respiratory syndrome

353
Anti-silencing function 1A histone chaperone
CGI-98, CIA, HSPC146
Melanoma

354
Armadillo repeat containing 8
GID5, HSPC056, S863-2, VID28
Myocardial infarction

355
ABI family member 3 binding protein
NESHBP, TARSH
Angioedema, Asthma, Basal cell carcinoma, Central nervous system cancer, Endometriosis, Glioma, Major depressive disorder, Oligodendroglioma, Open angle glaucoma, Depression, Urticaria

356
Alpha-1-microglobulin/bikunin precursor
A1M, EDC1, HCP, HI30, IATIL, ITI, ITIL, ITILC, UTI
Transitional cell carcinoma, Kidney failure, Mood disorder, Orofacial cleft

357
Anaphase promoting complex subunit 15
APC15, C11orf51, HSPC020
Deafness

358
ALS2 C-terminal like
RN49018
Coronary artery disease, Schizophrenia

359
Atlastin GTPase 3
AT3, ATL-3, HSN1F
Charcot-marie-tooth disease, Hereditary sensory and autonomic neuropathy, Hereditary sensory neuropathy

360
Assembly factor for spindle microtubules
ASP, Calmbp1, MCPH5
Arthrogryposis multiplex congenita, Primary microcephaly, Adenoid cystic carcinoma, Hepatocellular carcinoma, Congenital microcephaly, Congenital neurologic anomalies , Intellectual developmental disorder, Lissencephaly, Microcephaly, Pena-shokeir syndrome type i, Polycystic ovary syndrome, Salivary gland neoplasms