ERCC8 (gene)
Lua error in Module:Infobox_gene at line 33: attempt to index field 'wikibase' (a nil value). DNA excision repair protein ERCC-8 is a protein that in humans is encoded by the ERCC8 gene.[1][2]
This gene encodes a WD repeat protein, which interacts with the Cockayne syndrome type B (CSB) and p44 proteins, the latter being a subunit of the RNA polymerase II transcription factor II H. Mutations in this gene have been identified in patients with the hereditary disease Cockayne syndrome (CS). The CS cells are abnormally sensitive to ultraviolet radiation and are defective in the repair of transcriptionally active genes. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene.[2]
Interactions
ERCC8 (gene) has been shown to interact with XAB2.[3]
References
Further reading
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External links
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