CYP3A7

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

CYP3A7 is an enzyme belonging to the cytochrome P450 family. It is 503 amino acids in size and shares 87% of its sequence with CYP3A4. It carries out a similar role in fetuses that CYP3A4 serves in adults.[5] The gene location is 7q22.1.[6]

AliasesCYP3A7, CP37, CYPIIIA7, P-450(HFL33), P-450111A7, P450-HFLA, cytochrome P450 family 3 subfamily A member 7, P450HLp2
End99,735,196 bp[1]
Quick facts Identifiers, Aliases ...
CYP3A7
Identifiers
AliasesCYP3A7, CP37, CYPIIIA7, P-450(HFL33), P-450111A7, P450-HFLA, cytochrome P450 family 3 subfamily A member 7, P450HLp2
External IDsOMIM: 605340; MGI: 88610; HomoloGene: 133564; GeneCards: CYP3A7; OMA:CYP3A7 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_000765

NM_007819

RefSeq (protein)

NP_000756

NP_031845

Location (UCSC)Chr 7: 99.71 – 99.74 MbChr 5: 137.89 – 137.92 Mb
PubMed search[3][4]
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The CYP3A group of enzymes are the most abundantly expressed members of the cytochrome P450 family in liver. They are responsible for the metabolism of more than 50% of all clinical pharmaceuticals.[7]

The CYP3A7 enzyme hydroxylates testosterone and dehydroepiandrosterone 3-sulphate, which is involved in the formation of estriol during pregnancy. The CYP3A7 gene is part of a cluster of related genes on chromosome 7q21.1. Naturally occurring readthrough transcription occurs between this gene and the downstream CYP3A51P pseudogene.[8]

Notable alleles

The CYP3A7*1C allele is associated with poor outcomes in some cancer patients, possibly because of the effect of the enzyme on some chemotherapy agents.[9]

References

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