CSB Products

Description

ERCC6, also known as Cockayne syndrome B protein, is involved in DNA repair in response to UV exposure. ERCC6 has been reported to display ATPase and helicase activity and functions as a transcriptional regulator. Mutations in ERCC6 are the cause of Cockayne syndrome type B (CSB), cerebro-oculo-facio-skeletal syndrome type 1 (COFS1), De Sanctis-Cacchione syndrome (DCS), age-related macular degeneration type 5 (ARMD5), and UV-sensitive syndrome (UVS).

Bioinformatics

Entrez	2074 Human
Uniprot	NP_000115 Human NP_000115.1 Human
Product By Gene ID	2074
Alternate Names	ARMD5 ATP-dependent helicase ERCC6 CKN2 Cockayne syndrome group B protein Cockayne syndrome protein CSB COFS COFS1 CSBCockayne syndrome B protein DNA excision repair protein ERCC-6 EC 3.6.1 EC 3.6.4.- excision repair cross-complementing rodent repair deficiency, complementationgroup 6 Rad26 homolog RAD26

Research Areas for CSB

Find related products by research area and learn more about each of the different research areas below.

Cancer
DNA Repair
Nucleotide Excision Repair