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CYP20A1

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

CYP20A1 (cytochrome P450, family 20, subfamily A, polypeptide 1) is a protein which in humans is encoded by the CYP20A1 gene.[5]

AliasesCYP20A1, CYP-M, cytochrome P450 family 20 subfamily A member 1
External IDsMGI: 1925201; GeneCards: CYP20A1
End203,305,611 bp[1]
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CYP20A1
Identifiers
AliasesCYP20A1, CYP-M, cytochrome P450 family 20 subfamily A member 1
External IDsMGI: 1925201; GeneCards: CYP20A1
Orthologs
DatabasesNCBI: entry; OMA: entry
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_020674
NM_177538

NM_030013
NM_001313721

RefSeq (protein)

NP_001300650
NP_084289

Location (UCSC)Chr 2: 203.24 – 203.31 MbChr 1: 60.38 – 60.43 Mb
PubMed search[3][4]
Wikidata
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This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases that catalyze many reactions involved in pollutant and drug metabolism and the synthesis of cholesterol, steroids, and other lipids. CYP20A1 lacks one amino acid of the conserved heme binding site. It also lacks the conserved I-helix motif AGX(D,E)T, suggesting that its substrate may carry its own oxygen.[6]

CYP20A1 has no identified substrate or biological role and is considered an "orphan" P450.

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