FANCB, FA complementation group B

FANCB, FA complementation group B

• This gene encodes a member of the Fanconi anemia complementation group B. This protein is assembled into a nucleoprotein complex that is involved in the repair of DNA lesions. Mutations in this gene can cause chromosome instability and VACTERL syndrome with hydrocephalus. [provided by RefSeq, Apr 2016]

• Gene Synonyms (FA2, FAAP90, FAAP95, FAB, FACB, Fanconi anemia group B protein, Fanconi anemia complementation group B, Fanconi anemia-associated polypeptide of 95 kDa,)
• NCBI Gene ID: 2187
• Species: Homo sapiens (Human)
• UNIPROT ID#>>Q8NB91
  UNIPROT ID#>>A0A024RBW1
• View the NCBI Database for this Gene »

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

FA complementation group B interacts with:

• centromere protein S
  DnaJ heat shock protein family (Hsp40) member C7
  FA complementation group F
  FA complementation group G
  FA complementation group L
  FA complementation group M
  FA core complex associated protein 100
  FA core complex associated protein 20
  FA core complex associated protein 24
  Fanconi anemia core complex associated protein 100
  Fanconi anemia, complementation group C
  Fanconi anemia, complementation group L
  interleukin 6 receptor
  proteasome 20S subunit beta 3
  protein phosphatase 1 regulatory subunit 7
  thrombospondin 3
  ubiquitin conjugating enzyme E2 T
  vir like m6A methyltransferase associated

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.