QuickView for 4C3;jsessionid=D15401A2A3A388FA171FB9E2CFD3C184;jsessionid=BA6C8F6E4B4505572E2587E30F660038 (gene)

Gene Symbol:

CYP4V2 Homo sapiens

Full name:

cytochrome P450 family 4 subfamily V member 2

Synonyms:

BCD, CYP4AH1, cytochrome P450 4V2, cytochrome P450, family 4, subfamily V, polypeptide 2, docosahexaenoic acid omega-hydroxylase CYP4V2

Genomic Location:

Chr 4: 187349668-187371606

Description:

This gene encodes a member of the cytochrome P450 hemethiolate protein superfamily which are involved in oxidizing various substrates in the metabolic pathway. It is implicated in the metabolism of fatty acid precursors into n-3 polyunsaturated fatty acids. Mutations in this gene result in Bietti crystalline corneoretinal dystrophy.

This gene encodes a member of the cytochrome P450 hemethiolate protein superfamily which are involved in oxidizing various substrates in the metabolic pathway. It is implicated in the metabolism of fatty acid precursors into n-3 polyunsaturated fatty acids. Mutations in this gene result in Bietti crystalline corneoretinal dystrophy.

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Orthologs:

Mus musculus ,  Rattus norvegicus ,  D. melanogaster ,  C. elegans ,  Macaca mulatta ,  Gallus gallus ,  Bos taurus ,  Canis lupus familiaris ,  Pan troglodytes

External Links:

Entrez Gene

Transcription Factor
Binding Sites:

HEN1_01 ,  CTTTAAR_UNKNOWN ,  HEN1_02

Cytogenetic Map:

4q35.1-q35.2

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