ERCC4

该基因编码的蛋白质与ERCC1形成复合物,参与核苷酸切除修复过程中的5'切口。该复合物是一种与EME1相互作用的结构特异性DNA修复内切酶。该基因缺陷是着色性干皮病互补组F(xp-f)或着色性干皮病VI(xp6)的原因。[由Refseq提供,2009年3月]
The protein encoded by this gene forms a complex with ERCC1 and is involved in the 5' incision made during nucleotide excision repair. This complex is a structure specific DNA repair endonuclease that interacts with EME1. Defects in this gene are a cause of xeroderma pigmentosum complementation group F (XP-F), or xeroderma pigmentosum VI (XP6).[provided by RefSeq, Mar 2009]

别名

XPF,RAD1,FANCQ,XFEPS,ERCC11

基因id

Chromosome:16 Start: 14014014 End: 14046205 Strand: 

药物

突变与药物

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