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Gene : CYP4V2 Homo sapiens

Name  ? cytochrome P450 family 4 subfamily V member 2 Cytological Location  4q35.1-q35.2
Brief Description  cytochrome P450 family 4 subfamily V member 2
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. [provided by RefSeq, Jul 2008]
  • synonyms:
  • cytochrome P450, family 4, subfamily V, polypeptide 2,
  • HGNC:23198,
  • CYP4AH1,
  • NM_207352,
  • uc003iyw.5,
  • CYP4AH1,
  • AK022114,
  • CYP4V2,
  • BCD,
  • OTTHUMG00000160379
  • identifiers:
  • 285440,
  • ENSG00000145476,
  • CYP4V2

Genome feature

Region: gene ? Length: 21897  
Location: 4:186191567-186213463 Cyto location: 4q35.1-q35.2


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Proteins

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SNPs

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Disease

1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

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Expression

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3753 SN Ps

5 Cross References

18 Data Sets

32 Homologues

0 Located Features

97 Rna Seq Results