Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "A"
841 to 850 of 912 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

841
ADAM metallopeptidase domain 7
ADAM 7, ADAM-7, EAPI, GP-83, GP83

842
Actinin alpha 2
CMD1AA, CMH23, CMYO8, CMYP8, MPD6, MYOCOZ
Cardiac and skeletal myopathy, Arrhythmogenic right ventricular cardiomyopathy, Attention deficit hyperactivity disorder, Cardiomyopathy, Congenital myopathy, Dilated cardiomyopathy, Heart disease, Heart failure, Hypertrophic cardiomyopathy, Left ventricular noncompaction cardiomyopathy, Neuromuscular diseases, Periodontitis, Substance abuse, Ventricular fibrillation, Wolff-parkinson-white syndrome

843
ArfGAP with SH3 domain, ankyrin repeat and PH domain 2
AMAP2, CENTB3, DDEF2, PAG3, PAP, Pap-alpha, SHAG1
Ankylosing spondylitis, Asthma, Bipolar disorder, Central nervous system cancer, Obstructive pulmonary disease, Coronary artery disease, Crohn disease, Glioblastoma, Glioma, Gout, Multiple sclerosis, Neuroblastoma, Oligodendroglioma, Osteoarthritis, Psoriasis
View all (2 more)

844
Aldehyde dehydrogenase 1 family member A2
DIH4, RALDH(II), RALDH2, RALDH2-T
Alzheimer disease, Amyotrophic lateral sclerosis, Aortic stenosis, Aortic valve disease, Asthma, Atrial fibrillation, Atrophic macular degeneration, Barrett esophagus, Cancer, Cardiovascular disease, Coronary artery disease, Diabetes mellitus, Diaphragmatic malformations, Digestive system disease, Esophageal adenocarcinoma
View all (20 more)

845
Apelin
APEL, XNPEP2
Hepatocellular carcinoma, Cardiomegaly, Heart failure, Hyperuricemia, Hypotension

846
Actinin alpha 3
ACTN3D
Asthma, Bipolar disorder, Frontotemporal dementia, Insomnia, Sleep apnea, Ulcerative colitis

847
Adaptor related protein complex 1 subunit sigma 2
DC22, MRX59, MRXS21, MRXS5, MRXSF, PGS, SIGMA1B
Autism, Liver cirrhosis, Intellectual developmental disorder, x-linked, Partington syndrome, X-linked intellectual disability, X-linked complex neurodevelopmental disorder

848
Adaptor related protein complex 1 subunit mu 1
AP47, CLAPM2, CLTNM, MU-1A, mu1A

849
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-
Ataxia with polyneuropathy, Bicuspid aortic valve, Cardiomyopathy, Cerebellar ataxia, Cerebellar atrophy, Charcot-marie-tooth disease, Cleft palate and bilateral cleft lip, Diabetes mellitus, Gonadal dysgenesis, Hypertrophy, Systemic lupus erythematosus, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Multiple sclerosis
View all (8 more)

850
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-
Bicuspid aortic valve, Cardiomyopathy, Cerebellar ataxia, Cleft palate and bilateral cleft lip, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Multiple sclerosis, Neuropathy, ataxia, and retinitis pigmentosa, Leber hereditary optic neuropathy, Optic neuropathy, Periodic paralysis with later-onset distal motor neuropathy, Retinitis pigmentosa, Postaxial polydactyly