Genesⓘ

Dataset:
? Protein-coding genes with reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
401 to 410 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

401
Angiotensin II receptor associated protein
ATRAP
Schizophrenia

402
189
Alanine--glyoxylate aminotransferase
AGT, AGT1, AGXT1, PH1, SPAT, SPT, Ser-PyrAT, TLH6
Alanine-glyoxylate aminotransferase deficiency, Cardiac arrhythmia, Hyperoxaluria, Nephrolithiasis, Nephrotic syndrome, Oligodendroglioma

403
Alanine--glyoxylate aminotransferase 2
AGT2, BAIBA, DAIBAT
Atrial fibrillation, Beta-aminoisobutyric aciduria, Ischemic stroke, Ischemic heart disease, Congestive heart failure, Coronary artery disease, Heart failure, Hypertension, Claudication, Mild cognitive impairment, Myocardial ischemia, Systemic lupus erythematosus

404
AT-hook containing transcription factor 1
ELYS, MST108, MSTP108, TMBS62
Color vision deficiency, Intellectual developmental disorder, Strabismus

405
191
Adenosylhomocysteinase
SAHH, adoHcyase
Amino acid metabolism disorder, Androgenetic alopecia, S-adenosylhomocysteine hydrolase deficiency, Disorder of sulfur-bearing amino acid metabolism, Hepatic methionine adenosyltransferase deficiency, Hepatolenticular degeneration, Hypoxia, Nonalcoholic fatty liver disease, Venous thromboembolism

406
Adenosylhomocysteinase like 1
DCAL, IRBIT, PPP1R78, PRO0233, XPVKONA
Alzheimer disease, Attention deficit hyperactivity disorder, Metabolic syndrome, Ocular hypotension, Substance abuse, Diabetes mellitus, type 2

407
Adenosylhomocysteinase like 2
ADOHCYASE3, IRBIT2
Alzheimer disease, Color vision deficiency, Dementia, Prostatic neoplasm

408
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 disorder, Psoriasis, Sleep apnea, Xia-gibbs syndrome

409
Abelson helper integration site 1
AHI-1, JBTS3, ORF1, dJ71N10.1
Asthma, Eczema, Autism, Cerebellar diseases, Clonal hematopoiesis, Aplasia of the vermis, Global developmental delay, Hodgkin lymphoma, Selective immunoglobulin a deficiency, Intellectual developmental disorder, Joubert syndrome, Juvenile idiopathic arthritis, Leber congenital amaurosis, Multiple sclerosis, Nephronophthisis
View all (10 more)

410
AHNAK nucleoprotein
AHNAK1, AHNAKRS, PM227
Alzheimer disease, Bone fracture, Renal cell carcinoma, Chloracne, Obstructive pulmonary disease, Melanoma, Hypertrophic cardiomyopathy, Liver cirrhosis