Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "A"
381 to 390 of 912 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

381
Acyl-CoA dehydrogenase family member 8
ACAD-8, ARC42, IBDH
Isobutyryl-coa dehydrogenase deficiency, Obesity, Stomach neoplasms

382
Ankyrin repeat domain 1
ALRP, C-193, CARP, CVARP, MCARP, bA320F15.2
Dilated cardiomyopathy, Brugada syndrome, Cardiomyopathy, Congenital hemivertebra, Endometriosis, Hypertrophic cardiomyopathy, Left ventricular disease, Nemaline myopathy, Spinal muscular atrophy

383
Adenosine monophosphate deaminase 2
AMPD, PCH9, SPG63
Autoimmune thrombocytopenic purpura, Spastic paraplegia, Breast cancer, Congenital brain malformation, Congenital neurologic anomalies , Estrogen-receptor negative breast cancer, Global developmental delay, Hydranencephaly, Intellectual developmental disorder, Lissencephaly, Macrogyria, Microgyria, Pontocerebellar hypoplasia, Spastic ataxia, Hereditary spastic paraplegia

384
ALF transcription elongation factor 4
AF5Q31, CHOPS, MCEF
Bone disease, Cardiomyopathy, Chops syndrome, Cognition disorder, Congenital heart defects, Cornelia de lange syndrome, Delirium, dementia, and cognitive disorders, Growth disorder, Congenital heart defect, Lung disease, Obesity

385
Argonaute RISC catalytic component 2
CASC7, EIF2C2, LESKRES, LINC00980, PPD, Q10
Eczema, Glaucoma, Hearing loss, Heart failure, Hypertension, Hypothyroidism, Iron metabolism disorder, Myeloid leukemia, Mesothelioma, Metabolic syndrome, Neurodevelopmental disorders, Neurotic disorder, Non-specific syndromic intellectual disability, Premature ovarian failure, Diabetes mellitus, type 1
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386
Adenosine monophosphate deaminase 3
-
Myoadenylate deaminase deficiency, Atrial fibrillation, Bipolar disorder, Obstructive pulmonary disease, Color vision deficiency, Colorectal cancer, Melanoma, Hemorrhoid, Hypertension, Major depressive disorder, Intellectual developmental disorder, Nephrolithiasis, Osteoarthritis, Scoliosis

387
AT-hook DNA binding motif containing 1
MRD25, XIGIS
Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Coronary artery disease, Global developmental delay, Intellectual developmental disorder, Myocardial infarction, Neurodevelopmental disorders, Psoriasis, Sleep apnea

388
Amphiphysin
AMPH1
Scoliosis, Small vessel stroke

389
Angiopoietin like 3
ANG-5, ANGPT5, ANL3, FHBL2
Developmental and epileptic encephalopathy, Hypobetalipoproteinemia, Hypoalphalipoproteinemia, Liver cirrhosis

390
Apolipoprotein B mRNA editing enzyme catalytic subunit 3C
A3C, APOBEC1L, ARDC2, ARDC4, ARP5, PBI, bK150C2.3
Brain cancer, Brain neoplasms, Gestational diabetes, Non-organic psychosis, Psychotic disorders