ERCC5
Lua error in Module:Infobox_gene at line 33: attempt to index field 'wikibase' (a nil value). DNA repair protein complementing XP-G cells is a protein that in humans is encoded by the ERCC5 gene.[1][2]
Excision repair cross-complementing rodent repair deficiency, complementation group 5 (xeroderma pigmentosum, complementation group G) is involved in excision repair of UV-induced DNA damage. Mutations cause Cockayne syndrome, which is characterized by severe growth defects, mental retardation, and cachexia. Multiple alternatively spliced transcript variants encoding distinct isoforms have been described, but the biological validity of all variants has not been determined.[2]
Mutations in ERCC5 cause arthrogryposis .[3]
Interactions
ERCC5 has been shown to interact with ERCC2.[4]
References
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Further reading
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