OAT
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 10[13]
- Cytogenetic location
- 10q26.13[16]
- Expressed in
- jejunal mucosa, parotid gland, duodenum, secondary oocyte, epithelium of nasopharynx, pons, germinal epithelium, Brodmann area 23, mucosa of ileum, seminal vesicula[17][18][19][20][21][22][23][24][25][26]
- Found in taxon
- Homo sapiens[12]
- Genetic association
- gyrate atrophy of the choroid[14]
- HomoloGene ID
- 231[3]
- Strand orientation
- reverse strand[15]
🏷️ Also known as
en GACR
en HOGA
en OAT
en OATASE
en OKT
en ornithine aminotransferase
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000065154
- Ensembl transcript ID
- ENST00000539214, ENST00000368845, ENST00000467675, ENST00000471127, ENST00000476917, ENST00000483711, ENST00000490096, ENST00000492376
- Entrez Gene ID
- 4942
- Exact match
- identifiers.org
- Freebase ID
- /m/02r9_qf
- HGNC ID
- 8091
- HGNC gene symbol
- OAT
- OMIM ID
- 613349
- RefSeq RNA ID
- NM_000274, NM_001171814, NM_001322965, NM_001322966, NM_001322967, NM_001322968, NM_001322969, NM_001322970, NM_001322971, NM_001322974
- UMLS CUI
- C1417917
Press Enter · cited answer in seconds