Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "A"
361 to 370 of 912 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

361
AAR2 splicing factor
C20orf4, CGI-23
Cerebellar malformation, Global developmental delay, Non-melanoma skin carcinoma, Obesity, Ventricular septal defect

362
Amine oxidase copper containing 1
ABP, ABP1, DAO, DAO1, KAO, KDAO
Atrial fibrillation, Autism, Breast cancer, Cardiomegaly, Carpal tunnel syndrome, Diverticular disease, Gout, Hypertension, Metabolic syndrome, Osteoarthritis, Diabetes mellitus, type 2

363
Acyl-CoA thioesterase 11
BFIT, STARD14, THEA, THEM1
Pancreatic cancer

364
Attractin like 1
ALP, bA338L11.1, bA454H24.1
Attention deficit hyperactivity disorder, Bipolar disorder, Bone remodeling disease, Central nervous system cancer, Glioma, Huntington disease, Oligodendroglioma, Osteoarthritis, Ovarian cancer, Willis-ekbom disease

365
Activator of transcription and developmental regulator AUTS2
FBRSL2, MRD26
Alzheimer disease, Androgenetic alopecia, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, B-lymphoblastic leukemia/lymphoma, Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Color vision deficiency, Dementia, Developmental disability, Diabetes mellitus, Diabetes mellitus type 2, Diabetic eye disease, Dyslexia, Epilepsy
View all (15 more)

366
Ankyrin repeat domain 17
CAGS, GTAR, MASK2, NY-BR-16
Atrial fibrillation, Chopra-amiel-gordon syndrome, Intellectual developmental disorder, Non-specific syndromic intellectual disability, Smooth surface dental caries

367
Adaptor protein, phosphotyrosine interacting with PH domain and leucine zipper 1
APPL, DIP13alpha, MODY14
Liver cirrhosis, Major depressive disorder, Maturity-onset diabetes of the young (mody), Maturity-onset diabetes of the young

368
Rho guanine nucleotide exchange factor 26
CSGEF, HMFN1864, SGEF
Aortic stenosis, Colorectal cancer, Coronary artery disease, Gout, Myocardial infarction, Schizophrenia

369
Abhydrolase domain containing 12, lysophospholipase
ABHD12A, BEM46L2, C20orf22, PHARC, dJ965G21.2, hABHD12
Alzheimer disease, Charcot-marie-tooth disease, Cone dystrophy, Hearing impairment, Optic atrophy, Retinitis pigmentosa

370
ATP binding cassette subfamily A member 12
ARCI4A, ARCI4B, ICR2B, LI2
Atrial fibrillation, Attention deficit hyperactivity disorder, Congenital ichthyosis, Cancer, Carotid artery disease, Colorectal cancer, Colorectal neoplasm, Congenital nonbullous ichthyosiform erythroderma, Coronary artery disease, Diabetes mellitus, Heart failure, Ichthyosis, Lamellar ichthyosis, Stroke, Thyroid cancer