Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "A"
1031 to 1040 of 1170 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1031
Autophagy related 9B
APG9L2, NOS3AS, SONE
Premature ovarian failure

1032
5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/IMP cyclohydrolase
AICAR, AICARFT, HEL-S-70p, IMPCHASE, PURH
Aica-ribosiduria, Rheumatoid arthritis, Blindness, Kidney disease, Nephrotic syndrome, Osteoporosis, Spondylometaphyseal dysplasia

1033
Atlastin GTPase 1
AD-FSP, ATL-1, FSP1, GBP3, HSN1D, SPG3, SPG3A, atlastin1
Spastic paraplegia, Cardiovascular disease, Charcot-marie-tooth disease, Obstructive pulmonary disease, Congenital neurologic anomalies, Dupuytren contracture, Hereditary sensory and autonomic neuropathy, Potassium deficiency, Hereditary spastic paraplegia

1034
Atlastin GTPase 2
ARL3IP2, ARL6IP2, ATL-2, aip-2, atlastin2
Tourette syndrome, Insomnia

1035
Atlastin GTPase 3
AT3, ATL-3, HSN1F
Charcot-marie-tooth disease, Hereditary sensory and autonomic neuropathy

1036
ATM serine/threonine kinase
AT1, ATA, ATC, ATD, ATDC, ATE, TEL1, TELO1
Ataxia telangiectasia, B-cell chronic lymphocytic leukemia, Skin neoplasms, Breast neoplasms, Adenoid cystic carcinoma, Hepatocellular carcinoma, Squamous cell carcinoma, Cardiac valvular dysplasia, Dilated cardiomyopathy, Cataract, Cerebellar ataxia, Chromosome 17q21.31 deletion syndrome, Clonal hematopoiesis, Lynch syndrome, Conjunctival telangiectasis
View all (25 more)

1037
Atrophin 1
B37, CHEDDA, D12S755E, DRPLA, HRS, NOD
Congenital hypotonia, epilepsy, developmental delay, and digital anomalies, Dentatorubral pallidoluysian atrophy, Schizophrenia, X-linked hydrocephalus syndrome

1038
Atonal bHLH transcription factor 1
ATH1, DFNA89, HATH1, MATH-1, bHLHa14
Colorectal adenoma, Colorectal cancer, Deafness, Global developmental delay, Hearing loss, Medulloblastoma, Pontocerebellar hypoplasia, Schizophrenia, Diabetes mellitus type 2, Uterine fibroid

1039
Atonal bHLH transcription factor 7
Math5, NCRNA, PHPVAR, RNANC, bHLHa13
Alzheimer disease, Anterior segment dysgenesis, Congenital cataract microcornea with corneal opacity, Open angle glaucoma

1040
Atos homolog A
FAM214A, KIAA1370
Alzheimer disease, Dementia, Metabolic syndrome, Schizophrenia, Diabetes mellitus type 2