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Invitrogen
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Immunogen sequence: SCGCSSEFVF VPYGSTIAVY TVYSGEQITM LKGHYKTVDC CVFQSNFQEL YSGSRDCNIL AWVPSLYEPV PDDDETTTKS QLNPAFEDAW SSSDEEG; Positive Samples: Mouse testis; Cellular Location: Nucleus
This gene encodes a WD repeat protein, which interacts with Cockayne syndrome type B (CSB) protein and with p44 protein, a subunit of the RNA polymerase II transcription factor IIH. Mutations in this gene have been identified in patients with hereditary disease Cockayne syndrome (CS). CS cells are abnormally sensitive to ultraviolet radiation and are defective in the repair of transcriptionally active genes.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: Cockayne syndrome 1 homolog; Cockayne syndrome WD repeat protein CSA homolog; DNA excision repair protein ERCC-8
基因别名: 2410022P04Rik; 2810431L23Rik; 4631412O06Rik; B130065P18Rik; Ckn1; Csa; Ercc8
UniProt ID: (Mouse) Q8CFD5
Entrez Gene ID: (Mouse) 71991