CYP4V2

CYP4V2
Identifiers
Aliases	CYP4V2, BCD, CYP4AH1, cytochrome P450 family 4 subfamily V member 2
External IDs	OMIM: 608614; MGI: 2142763; HomoloGene: 133054; GeneCards: CYP4V2; OMA:CYP4V2 - orthologs
EC number	1.14.14.79
Gene location (Human)
Chr.	Chromosome 4 (human)
End	186,213,463 bp
Gene location (Mouse)
Chr.	Chromosome 8 (mouse)
End	45,786,253 bp
RNA expression pattern
	Top 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;
	Top expressed in
	left lobe of liver; ; jejunum; ; intestinal villus; ; epithelium of lens; ; Ileal epithelium; ; duodenum; ; Paneth cell; ; olfactory epithelium; ; vestibular membrane of cochlear duct; ; sciatic nerve;
	More reference expression data
	n/a
Gene ontology
Molecular function	metal ion binding; iron ion binding; oxidoreductase activity; heme binding; oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen; monooxygenase activity;
Cellular component	integral component of membrane; endoplasmic reticulum membrane; endoplasmic reticulum; membrane;
Biological process	response to stimulus; sterol metabolic process; fatty acid omega-oxidation; visual perception; retinoid metabolic process; lipid metabolism;
	Sources:Amigo / QuickGO
Orthologs
	285440
	102294
	ENSG00000145476
	ENSMUSG00000079057
	Q6ZWL3
	Q9DBW0
	NM_207352
	NM_133969
	NP_997235
	NP_598730
	Wikidata
View/Edit Human	View/Edit Mouse

Cytochrome P450 4V2 is a protein that in humans is encoded by the CYP4V2 gene.

Mutations are associated with Bietti's crystalline dystrophy and retinitis pigmentosas.