CYP4V2
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 4[16]
- Cytogenetic location
- 4q35.1-q35.2[19]
- Expressed in
- mucosa of ileum, liver, pancreatic epithelial cell, right lobe of liver, jejunal mucosa, retinal pigment epithelium, cardiac muscle tissue of right atrium, islet of Langerhans, gallbladder, right adrenal cortex[20][21][22][23][24][25][26][27][28][29]
- Found in taxon
- Homo sapiens[15]
- Genetic association
- Bietti crystalline corneoretinal dystrophy[17]
- HomoloGene ID
- 133054[3]
- Strand orientation
- forward strand[18]
🏷️ Also known as
en BCD
en CYP4AH1
en CYP4V2
en cytochrome P450 family 4 subfamily V member 2
ar CYP٤V٢
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000145476
- Ensembl transcript ID
- ENST00000513354, ENST00000378802, ENST00000502665, ENST00000507209
- Entrez Gene ID
- 285440
- Exact match
- identifiers.org
- Freebase ID
- /m/03hgknk
- HGNC ID
- 23198
- HGNC gene symbol
- CYP4V2
- OMIM ID
- 608614
- RefSeq RNA ID
- NM_207352, XM_005262935, XM_047450077
- UMLS CUI
- C1539212
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