MeSH Browser

MeSH Supplementary: CYP4V2 protein, human
Unique ID: C505357
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C505357
Entry Term(s): cytochrome P-450 CYP4V2, human; cytochrome P450, family 4, subfamily V, polypeptide 2, human
Registry Numbers: EC 1.14.13.-
Previous Indexing: *CYTOCHROME P-450 ENZYME SYSTEM (2005-2016)
Heading Mapped to: *Cytochrome P450 Family 4
Frequency: 72
Note: mutations of the CYP4V2 gene on chromosome 4q35 are associated with Bietti crystalline dystrophy; RefSeq NM_207352
Source: Invest Ophthalmol Vis Sci 2005 Oct;46(10):3812-6
Date of Entry: 2005/11/17
Revision Date: 2016/06/29

CYP4V2 protein, human MeSH Supplementary Concept Data 2025