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) Band 4q35.1-q35.2 Start 186,191,567 bp End 186,213,463 bp
Gene location (Mouse) Chr. Chromosome 8 (mouse) Band 8|8 B1.1 Start 45,757,981 bp End 45,786,253 bp
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in liver pancreatic epithelial cell right lobe of liver jejunal mucosa retinal pigment epithelium islet of Langerhans gallbladder renal medulla body of pancreas visceral pleura Top expressed in left lobe of liver jejunum intestinal villus duodenum Paneth cell olfactory epithelium sciatic nerve right lung lobe substantia nigra carotid body More reference expression data BioGPS 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 Species Human Mouse Entrez 285440 102294 Ensembl ENSG00000145476 ENSMUSG00000079057 UniProt Q6ZWL3 Q9DBW0 RefSeq (mRNA) NM_207352 NM_133969 RefSeq (protein) NP_997235 NP_598730 Location (UCSC) Chr 4: 186.19 – 186.21 Mb Chr 8: 45.76 – 45.79 Mb PubMed search
Wikidata
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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.

Further reading

• Jiao X, Munier FL, Iwata F, et al. (2000). "Genetic linkage of Bietti crystallin corneoretinal dystrophy to chromosome 4q35". Am. J. Hum. Genet. 67 (5): 1309–13. doi:10.1016/S0002-9297(07)62960-7. PMC 1288572. PMID 11001583.
• Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
• Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
• Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
• Wada Y, Itabashi T, Sato H, et al. (2005). "Screening for mutations in CYP4V2 gene in Japanese patients with Bietti's crystalline corneoretinal dystrophy". Am. J. Ophthalmol. 139 (5): 894–9. doi:10.1016/j.ajo.2004.11.065. PMID 15860296.
• Gekka T, Hayashi T, Takeuchi T, et al. (2005). "CYP4V2 mutations in two Japanese patients with Bietti's crystalline dystrophy". Ophthalmic Res. 37 (5): 262–9. doi:10.1159/000087214. PMID 16088246.
• Shan M, Dong B, Zhao X, et al. (2006). "Novel mutations in the CYP4V2 gene associated with Bietti crystalline corneoretinal dystrophy". Mol. Vis. 11: 738–43. PMID 16179904.
• Lee KY, Koh AH, Aung T, et al. (2005). "Characterization of Bietti crystalline dystrophy patients with CYP4V2 mutations". Invest. Ophthalmol. Vis. Sci. 46 (10): 3812–6. doi:10.1167/iovs.05-0378. PMID 16186368.
• Jin ZB, Ito S, Saito Y, et al. (2006). "Clinical and molecular findings in three Japanese patients with crystalline retinopathy". Jpn. J. Ophthalmol. 50 (5): 426–31. doi:10.1007/s10384-006-0350-0. PMID 17013694.
• Nakamura M, Lin J, Nishiguchi K, et al. (2007). Bietti crystalline corneoretinal dystrophy associated with CYP4V2 gene mutations. Advances in Experimental Medicine and Biology. Vol. 572. pp. 49–53. doi:10.1007/0-387-32442-9_8. ISBN 978-0-387-28464-4. PMID 17249554. {{cite book}}: |journal= ignored (help)
• Lai TY, Ng TK, Tam PO, et al. (2007). "Genotype phenotype analysis of Bietti's crystalline dystrophy in patients with CYP4V2 mutations". Invest. Ophthalmol. Vis. Sci. 48 (11): 5212–20. doi:10.1167/iovs.07-0660. PMID 17962476.