1. Gene
  2. Fancb - Fanconi anemia, complementation group B Gene

Fancb - Fanconi anemia, complementation group B Gene

Mus musculus
Gene ID: 237211 | Gene type: protein coding

About Fancb

Summary

Acts upstream of or within several processes, including cellular response to camptothecin; regulation of double-strand break repair via homologous recombination; and replication-born double-strand break repair via sister chromatid exchange. Predicted to be located in nucleus. 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(2)

mRNA Protein Name
NM_001146081.2 NP_001139553.1 Fanconi anemia group B protein homolog isoform 1
NM_175027.5 NP_778192.3 Fanconi anemia group B protein homolog isoform 2
Gene Ontology
  • Biological Process
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

Fanconi anemia group B protein homolog

Orthologs Information

Species Symbol Source ID
Homo sapiens Fancb NCBI NCBI:2187