2. Gene
  3. Fancb - FA complementation group B Gene

Fancb - FA complementation group B Gene

  • Gene
  • Protein
  • Agent
  • Ortholog
Rattus norvegicus

Also known as RGD1561555

Gene ID: 501552 | Gene type: protein coding

About Fancb

Summary

Predicted to be involved in negative regulation of double-strand break repair via homologous recombination; positive regulation of double-strand break repair via homologous recombination; and replication-born double-strand break repair via sister chromatid exchange. Predicted to act upstream of or within cellular response to camptothecin and cellular response to xenobiotic stimulus. Predicted to be part of Fanconi anaemia nuclear complex. Human ortholog(s) of this gene implicated in Fanconi anemia complementation group B and head and neck squamous cell carcinoma. Orthologous to human FANCB (FA complementation group B). [provided by Alliance of Genome Resources, Apr 2022]

Fancb Products(1)

mRNA Protein Name
NM_001192003.1 NP_001178932.1 Fanconi anemia group B protein
Protein Preferred Names Protein Names

Fanconi anemia group B protein

Fanconi anemia, complementation group B

Related Agents

Pre-clinical Phase
Bioactive Molecules (1)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-RS04733 FANCB Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Homo sapiens Fancb NCBI NCBI:2187