LRAT
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 4[13]
- Cytogenetic location
- 4q32.1[16]
- Expressed in
- retinal pigment epithelium, testicle, gonad, gallbladder, jejunal mucosa, C1 segment, duodenum, right lobe of liver, muscle layer of sigmoid colon, tibial nerve[17][18][19][20][21][22][23][24][25][26]
- Found in taxon
- Homo sapiens[12]
- Genetic association
- Leber congenital amaurosis 14[14]
- HomoloGene ID
- 3483[3]
- Strand orientation
- forward strand[15]
🏷️ Also known as
en LCA14
en lecithin retinol acyltransferase
en lecithin retinol acyltransferase (phosphatidylcholine--retinol O-acyltransferase)
en LRAT
🔖 Identifiers · 9
- Ensembl gene ID
- ENSG00000121207
- Ensembl transcript ID
- ENST00000510919, ENST00000336356, ENST00000499392, ENST00000500890, ENST00000502474, ENST00000502525, ENST00000507827, ENST00000510733
- Entrez Gene ID
- 9227
- Exact match
- identifiers.org
- HGNC ID
- 6685
- HGNC gene symbol
- LRAT
- OMIM ID
- 604863
- RefSeq RNA ID
- NM_001301645, NM_004744, XM_047416405
- UMLS CUI
- C1416905
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