Xeroderma Pigmentosum Group C Complementing factor [Homo sapiens]

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Structural modeling and analyses of genetic variations in the human XPC nucleotide excision repair protein. [J Biomol Struct Dyn. 2023]
Structural modeling and analyses of genetic variations in the human XPC nucleotide excision repair protein.
Le J, Min JH. J Biomol Struct Dyn. 2023; 41(23):13535-13562. Epub 2023 Mar 8.
Association between polymorphisms rs2228001 and rs2228000 in XPC and genetic susceptibility to preeclampsia: a case control study. [BMC Pregnancy Childbirth. 2021]
Association between polymorphisms rs2228001 and rs2228000 in XPC and genetic susceptibility to preeclampsia: a case control study.
Wang J, Guan C, Sui J, Zang Y, Wu Y, Zhang R, Qi X, Piao S. BMC Pregnancy Childbirth. 2021 Nov 22; 21(1):787. Epub 2021 Nov 22.
Loss of Function Variants in the XPC Causes Severe Xeroderma Pigmentosum in Three Large Consanguineous Families. [Klin Padiatr. 2022]
Loss of Function Variants in the XPC Causes Severe Xeroderma Pigmentosum in Three Large Consanguineous Families.
Nawal W, Ullah A, Ullah U, Farrakh K, Ahmad F, Khan H, Ahmad GS, Khan B, Ansar M, Kalsoom UE, et al. Klin Padiatr. 2022 May; 234(3):123-129. Epub 2021 Sep 20.

RefSeq genomic sequence
See the genomic reference sequence for the XPC gene (NG_011763.1).
RefSeq protein isoforms
See 9 reference sequence protein isoforms for the XPC gene.

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Transcript/Protein Information [PANTHER Classification System]
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reagent reviews [ExactAntigen/Labome]
reagent reviews
ExactAntigen/Labome
reagents [ExactAntigen/Labome]
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