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"
761 to 770 of 1170 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

761
Apolipoprotein L4
APOL-IV, APOLIV
Kidney disease, Nephrotic syndrome, Schizophrenia

762
Apolipoprotein L6
APOL-VI, APOLVI
Colonic neoplasms

763
Apolipoprotein L domain containing 1
BDVAS, VERGE
Atrial fibrillation, Platelet-type bleeding disorder, Blood coagulation disorder, Cardiovascular disease, Hypertension, Prostate cancer

764
Apolipoprotein M
G3a, HSPC336, NG20, apo-M
Ischemic heart disease, Coronary artery disease, Diabetes mellitus type 1, Diabetes mellitus type 2, Lung cancer, Myocardial ischemia, Non-small cell lung carcinoma, Rheumatoid arthritis, Sarcoidosis, Squamous cell carcinoma, Upper aerodigestive tract neoplasm

765
Apolipoprotein O
FAM121B, MIC26, MICOS26, Mic23, My025
Gestational diabetes, Mitochondrial disease

766
Amyloid beta precursor protein
AAA, ABETA, ABPP, AD1, APPI, CTFgamma, CVAP, PN-II, PN2, alpha-sAPP, preA4
Abeta amyloidosis, Alzheimer disease, Amnesia, Amyloid angiopathy, Amyloid neuropathy, Amyloidosis, Anxiety disorder, Bipolar disorder, Brain disease, Cardiomyopathy, Cerebral amyloid angiopathy, Cerebral hemorrhage, Lymphocytic leukemia, Cognition disorder, Degenerative disorder
View all (16 more)

767
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

768
Adaptor protein, phosphotyrosine interacting with PH domain and leucine zipper 2
DIP13B
Prostatic neoplasms

769
Adenine phosphoribosyltransferase
AMP, APRTD
2,8-dihydroxyadenine urolithiasis, Adenine phosphoribosyltransferase deficiency, Breast neoplasms, Renal cell carcinoma, Major depressive disorder, Mucopolysaccharidosis, Depression, Urolithiasis

770
Aprataxin
AOA, AOA1, AXA1, EAOH, EOAHA, FHA-HIT
Amyotrophic lateral sclerosis, Ataxia with oculomotor apraxia, Coenzyme q10 deficiency, Ataxia with oculomotor apraxia and hypoalbuminemia, Epilepsy, Peripheral neuropathy, Schizophrenia, Spinocerebellar ataxia