Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "A"
761 to 770 of 912 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

761
Adrenomedullin 2
AM2, dJ579N16.4
Myocardial ischemia, Vascular disease

762
Alpha tubulin acetyltransferase 1
C6orf134, MEC17, Nbla00487, TAT, alpha-TAT, alpha-TAT1
Autism, Major depressive disorder, Prostate cancer, Schizophrenia, Myopia

763
ADAM metallopeptidase with thrombospondin type 1 motif 20
ADAM-TS20, ADAMTS-20, GON-1
Alzheimer disease, Insomnia, Melanoma, Diabetes mellitus, type 2

764
Asparaginase and isoaspartyl peptidase 1
ALP, ALP1, CRASH
Obstructive pulmonary disease, Allergic contact dermatitis, Retinitis pigmentosa

765
Armadillo repeat containing 9
ARM, JBTS30, KU-MEL-1, NS21
Dandy-walker syndrome, Diabetes mellitus, Diverticular disease, Aplasia of the vermis, Joubert syndrome, Multiple myeloma, Systemic lupus erythematosus

766
Alpha kinase 1
8430410J10Rik, LAK, ROSAH
Gouty arthritis, Atrial fibrillation, Diabetes mellitus, Diabetic neuropathy, Eye disease, Gout, Insomnia, Nephrosclerosis, Obesity, Retinitis pigmentosa, Rheumatoid arthritis

767
ADAM metallopeptidase domain 33
C20orf153, DJ964F7.1
Asthma, Breast neoplasm, Bronchial hyperreactivity, Obstructive airway disease, Obstructive pulmonary disease, Rhinitis, Urinary system disease

768
ADAM metallopeptidase domain 12
ADAM12-OT1, CAR10, MCMP, MCMPMltna, MLTN, MLTNA
Bipolar disorder, Color vision deficiency, Endometrial cancer, Endometrial neoplasm, Hypogonadism, Major depressive disorder, Schizophrenia

769
Acyl-CoA dehydrogenase family member 10
-
Atrial fibrillation, Atrophic macular degeneration, Kidney disease, Obstructive pulmonary disease, Colorectal cancer, Coronary artery disease, Esophageal cancer, Gout, Graves disease, Heart failure, Kidney failure, Major depressive disorder, Myocardial infarction, Stroke, Diabetes mellitus, type 2
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770
ASXL transcriptional regulator 3
BRPS, KIAA1713
Asthma, Autism, Bipolar disorder, Color vision deficiency, Epilepsy, Global developmental delay, Heart failure, Insomnia, Intellectual developmental disorder, Major depressive disorder, Metabolic syndrome, Neurodevelopmental disorders, Neurotic disorder, Ovarian cancer, Parkinson disease
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