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BRCA2 gene

BRCA2 DNA repair associated

Key facts

Official symbol
BRCA2
Full name
BRCA2
Chromosome
13
Map location
13q13.1
Organism
Homo sapiens
NCBI Gene ID
675
Also known as
BRCC2, BROVCA2, FACD, FAD, FAD1, FANCD

Function summary

The product of this gene in involved in maintenance of genome stability. It is involved in double-strand break repair pathways during mitotic and meiotic homologous recombination and functions in protecting DNA replication forks. The encoded protein contains sites for interactions with PALB2 and EMSY and an N-terminal DNA binding domain. It also contains a RAD51 binding domain with multiple components. It has multiple BRC repeats, an alpha helix domain, oligonucleotide binding folds, and a tower-like domain. It has a nuclear localization signal and a phosphorylation site for cyclin-dependent kinase. The C-terminus of the protein can bind single-stranded and double-stranded DNA. The product of this gene interacts with multiple proteins, including RAD51. It is involved in recruiting RAD51 filaments to DNA double-strand break sites and also in cytoplasmic division. It also acts as a tumor suppressor. Mutations in this gene or decreased expression have been implicated in multiple tumor types, including breast, ovarian, pancreatic, prostate and other cancers. [provided by RefSeq, May 2026].

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Data source: NCBI Gene · alsesAI Gene Library