Pages
Products

C1ORF124


Official Full Name
SprT-like N-terminal domain
Organism
Homo sapiens
Gene ID
83932
Background
The protein encoded by this gene may play a role in DNA repair during replication of damaged DNA. This protein recruits valosin containing protein (p97) to stalled DNA replication forks where it may prevent excessive translesional DNA synthesis and limit the number of DNA-damage induced mutations. It may also be involved in replication-related G2/M-checkpoint regulation. Deficiency of a similar protein in mouse causes chromosomal instability and progeroid phenotypes. Mutations in this gene have been associated with Ruijs-Aalfs syndrome (RJALS). Alternatively spliced transcript variants have been identified. [provided by RefSeq, Mar 2015]
Synonyms
SPRTN; DVC1; PRO4323; spartan; C1orf124

Cat.No. Product Name Price
SHH250362 shRNA set against Human C1orf124 (NM_032018.5) Inquiry
Cat.No. Product Name Price
MiUTR3H-14047 SPRTN miRNA 3'UTR clone Inquiry
CDCB187015 Rabbit SPRTN ORF clone (XM_002717370.2) Inquiry
CDCS419625 Human SPRTN ORF Clone (BC015740) Inquiry
CDCS419626 Human SPRTN ORF Clone (BC068478) Inquiry
Quick Inquiry