Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "A"
471 to 480 of 912 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

471
A-Raf proto-oncogene, serine/threonine kinase
A-RAF, ARAF1, PKS2, RAFA1
Breast neoplasm, Diffuse lymphatic malformation

472
Acyl-CoA dehydrogenase very long chain
ACAD6, LCACD, VLCAD
Autism, Cardiac arrhythmia, Cardiomyopathy, Hearing loss, Hypoxia, Intellectual developmental disorder, Myopathy, Very long chain acyl-coa dehydrogenase deficiency, Very long-chain acyl-coa dehydrogenase deficiency, Yorifuji okuno syndrome

473
Archain 1 coat protein complex I subunit delta
COPD, SRMMD, SSMG
Ataxia, Desbuquois syndrome

474
Anosmin 1
ADMLX, HH1, HHA, KAL, KAL1, KALIG-1, KMS, WFDC19
Hypogonadotropic hypogonadism, Hypopituitarism, Growth hormone deficiency, Kallmann syndrome, Martsolf syndrome, Micropenis, Panhypopituitarism, Pituitary dwarfism, Pituitary short stature, Severe acute respiratory syndrome, Sheehan syndrome

475
Amphiregulin
AR, AREGB, CRDGF, SDGF
Androgenetic alopecia, Juvenile arthritis, Asthma, Breast neoplasm, Non-small-cell lung carcinoma, Squamous cell carcinoma, Endometriosis, Head and neck neoplasm, Hemorrhoid, Juvenile idiopathic arthritis, Myocardial ischemia, Ovarian neoplasm, Oligoarticular juvenile idiopathic arthritis, Erythropoietic protoporphyria, Pulmonary fibrosis
View all (2 more)

476
Asparaginase
C14orf76, GPA/WT, LYSOLP, hASNase1
Anaphylaxis, Anemia, Stone disease, Hepatocellular carcinoma, Cholecystolithiasis, Hematuria, Schizophrenia, Vomiting

477
ATPase phospholipid transporting 9B (putative)
ATPASEP, ATPIIB, HUSSY-20, NEO1L, hMMR1
Color vision deficiency, Frontotemporal dementia, Prostate cancer

478
ARF GTPase 1
PVNH8
Breast neoplasm, Charcot-marie-tooth disease, Periventricular heterotopia, x-linked, Periventricular nodular heterotopia, Scoliosis

479
Agrin
AGRIN, CMS8, CMSPPD
Alzheimer disease, Atrial fibrillation, Presynaptic congenital myasthenic syndromes, Congenital myasthenic syndrome, Hyperopia, Myeloid leukemia, Myasthenic syndrome, Neurodevelopmental disorders, Postsynaptic congenital myasthenic syndrome, Presynaptic congenital myasthenic syndrome

480
Acetyl-CoA acetyltransferase 1
ACAT, MAT, T2, THIL
Beta-ketothiolase deficiency, Carbohydrate metabolism disease, Acetyl-coa acetyltransferase deficiency, Kidney failure, Liver cirrhosis, Seizures