SCUBA

RAD51B — RAD51 paralog B

RAD51B belongs to a gene co-expression module in 3 of 28 SCUBA cell types. Each module groups genes that rise and fall together in that cell type; the genes it shares a module with are its closest co-expression partners there.

RAD51B's module in each cell type

Cell typeModuleShares the module with
EnterocytesLong-gene transcript bias
Technical artifact
CBLB, CSTPP1, GALNT6, GSDME, LARGE1, PLXNA2View in SCUBA
Mucosal-associated invariant T cellChromatin Remodeling
DNA/chromatin regulation
ANK3, ARHGAP15, ARL15, BCAS3, CAMKMT, CCDC91, DPYD, EDA +13 more
NeutrophilsGeneral Homeostatic Regulation
Housekeeping
ARID2, EXOC4, FBXL17, LARP4B, MCU, MGAT5, RASA1

About the gene

SynonymshREC2, R51H2, RAD51L1, REC2
Chromosome14: 67819779-68730218
Predicted locationIntracellular, Membrane
Essential geneNo
Protein classCancer-related genes, Disease related genes, Predicted intracellular proteins, Predicted membrane proteins
Molecular functionDNA-binding
Biological processDNA damage, DNA recombination, DNA repair

Function

Involved in the homologous recombination repair (HRR) pathway of double-stranded DNA breaks arising during DNA replication or induced by DNA-damaging agents. May promote the assembly of presynaptic RAD51 nucleoprotein filaments. Binds single-stranded DNA and double-stranded DNA and has DNA-dependent ATPase activity. Part of the RAD51 paralog protein complex BCDX2 which acts in the BRCA1-BRCA2-dependent HR pathway. Upon DNA damage, BCDX2 acts downstream of BRCA2 recruitment and upstream of RAD51 recruitment. BCDX2 binds predominantly to the intersection of the four duplex arms of the Holliday junction and to junction of replication forks. The BCDX2 complex was originally reported to bind single-stranded DNA, single-stranded gaps in duplex DNA and specifically to nicks in duplex DNA. The BCDX2 subcomplex RAD51B:RAD51C exhibits single-stranded DNA-dependent ATPase activity suggesting an involvement in early stages of the HR pathway.

Human Protein Atlas · Open Targets · UniProt

Gene annotation from the Human Protein Atlas and UniProt; see sources & licences.