RDH5
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene[2]
- Chromosome
- human chromosome 12[14]
- Cytogenetic location
- 12q13.2[17]
- Encodes
- Retinol dehydrogenase 5, 11-cis retinol dehydrogenase[11][12]
- Expressed in
- subcutaneous adipose tissue, right lobe of liver, mucosa of transverse colon, right auricle of heart, duodenum, muscle layer of sigmoid colon, left coronary artery, left ventricle, lactiferous gland, muscle of thigh[18][19][20][21][22][23][24][25][26][27]
- Found in taxon
- Homo sapiens[13]
- Genetic association
- fundus dystrophy[15]
- HomoloGene ID
- 2179[3]
- Strand orientation
- forward strand[16]
🏷️ Also known as
en 9cRDH
en HSD17B9
en RDH1
en RDH5
en retinol dehydrogenase 5
en SDR9C5
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000135437
- Ensembl transcript ID
- ENST00000553187, ENST00000257895, ENST00000547072, ENST00000547301, ENST00000548082, ENST00000548123, ENST00000548486, ENST00000550608, ENST00000551444, ENST00000552930, ENST00000553160
- Entrez Gene ID
- 5959
- Exact match
- identifiers.org
- Freebase ID
- /m/03gxc3b
- HGNC ID
- 9940
- HGNC gene symbol
- RDH5
- OMIM ID
- 601617
- RefSeq RNA ID
- NM_002905, NM_001199771
- UMLS CUI
- C1419328
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Summary
RDH5 is a gene[1].