CYP26C1

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

CYP26C1

CYP26C1 (cytochrome P450, family 26, subfamily c, polypeptide 1) is a protein which in humans is encoded by the CYP26C1 gene.[5]

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CYP26C1
Identifiers
AliasesCYP26C1, FFDD4, cytochrome P450 family 26 subfamily C member 1
External IDsOMIM: 608428; MGI: 2679699; HomoloGene: 28089; GeneCards: CYP26C1; OMA:CYP26C1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_183374

NM_001105201

RefSeq (protein)

NP_899230

NP_001098671

Location (UCSC)Chr 10: 93.06 – 93.07 MbChr 19: 37.67 – 37.68 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 which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This enzyme is involved in the catabolism of all-trans- and 9-cis-retinoic acid, and thus contributes to the regulation of retinoic acid levels in cells and tissues.[6]

CYP26C1 was found to show no expression in colorectal cancer cells or normal colonic epithelium.[7]

References

Further reading

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