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"
931 to 940 of 1165 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

931
Arylsulfatase family member K
MPS10, TSULF
Autism, Mucopolysaccharidosis

932
Arylsulfatase L
ARSE, ASE, CDPX, CDPX1, CDPXR
Autism, Brachytelephalangic chondrodysplasia punctata, Chondrodysplasia, Coffin-siris syndrome, Connective tissue disease, Desbuquois syndrome, X-linked chondrodysplasia punctata

933
ADP-ribosyltransferase 1
ART2, ARTC1, CD296, RT6
Colorectal cancer, Colorectal adenoma

934
ADP-ribosyltransferase 3 (inactive)
ARTC3
Metabolic syndrome, Diabetes mellitus type 2

935
Artemin
ART, ENOVIN, EVN, NBN
Breast neoplasms, Major depressive disorder, Atopic dermatitis, Pruritus, Depression

936
ARV1 fatty acid homeostasis modulator
DEE38, EIEE38
Blindness, Congenital neurologic anomalies, Developmental and epileptic encephalopathy

937
ARVCF delta catenin family member
-
22q11.2 deletion syndrome, Alzheimer disease, Coronary artery disease, Digeorge syndrome, Raynaud disease, Schizophrenia, Diabetes mellitus type 2

938
Aristaless related homeobox
CT121, EIEE1, ISSX, MRX29, MRX32, MRX33, MRX36, MRX38, MRX43, MRX54, MRX76, MRX87, MRXS1, PRTS
Arachnoid cysts, Autism, Corpus callosum agenesis with abnormal genitalia, Developmental and epileptic encephalopathy, Hydranencephaly, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Lissencephaly, x-linked, X-linked intellectual disability, Partington syndrome, Periventricular heterotopia, Russell-silver syndrome, West syndrome, X-linked complex neurodevelopmental disorder, X-linked lissencephaly
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939
Arsenite methyltransferase
CYT19
Alzheimer disease, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Coronary artery disease, Developmental disability, Insomnia, Diabetes mellitus type 2, Lung neoplasms, Major depressive disorder, Obesity, Myocardial infarction, Neurotic disorder, Schizophrenia, Skin disease
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940
N-acylsphingosine amidohydrolase 1
AC, ACDase, ASAH, PHP, PHP32, SMAPME
Arthrogryposis multiplex congenita, Atrial fibrillation, Atrial flutter, Cardiac arrhythmia, Schizophrenia, Congenital neurologic anomalies, Rolandic epilepsy, Farber disease, Lipidoses, Lipoidosis, Oligodendroglioma, Pena-shokeir syndrome , Spinal muscular atrophy, Diabetes mellitus type 2