RAD51B
DNA repair protein RAD51 homolog 2
Also known as: hREC2, R51H2, RA51B_HUMAN, RAD51L1, REC2
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O15315
- Gene
- RAD51B
- Ensembl
- ENSG00000182185
- Chromosome
- 14
- Canonical length
- 384 aa
- Protein class
- Cancer-related genes, Disease related genes, Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Nucleoplasm,Nuclear bodies
OverviewNCBI Gene
The protein encoded by this gene is a member of the RAD51 protein family. RAD51 family members are evolutionarily conserved proteins essential for DNA repair by homologous recombination. This protein has been shown to form a stable heterodimer with the family member RAD51C, which further interacts with the other family members, such as RAD51, XRCC2, and XRCC3. Overexpression of this gene was found to cause cell cycle G1 delay and cell apoptosis, which suggested a role of this protein in sensing DNA damage. Rearrangements between this locus and high mobility group AT-hook 2 (HMGA2, GeneID 8091) have been observed in uterine leiomyomata. [provided by RefSeq, Mar 2016]
Canonical amino-acid sequenceUniProt
384 residues, UniProt reviewed canonical sequence.
>O15315|RAD51B
1 MGSKKLKRVG LSQELCDRLS RHQILTCQDF LCLSPLELMK VTGLSYRGVH ELLCMVSRAC
61 APKMQTAYGI KAQRSADFSP AFLSTTLSAL DEALHGGVAC GSLTEITGPP GCGKTQFCIM
121 MSILATLPTN MGGLEGAVVY IDTESAFSAE RLVEIAESRF PRYFNTEEKL LLTSSKVHLY
181 RELTCDEVLQ RIESLEEEII SKGIKLVILD SVASVVRKEF DAQLQGNLKE RNKFLAREAS
241 SLKYLAEEFS IPVILTNQIT THLSGALASQ ADLVSPADDL SLSEGTSGSS CVIAALGNTW
301 SHSVNTRLIL QYLDSERRQI LIAKSPLAPF TSFVYTIKEE GLVLQETTFC SVTQAELNWA
361 PEILPPQPPE QLGLQMCHHT QLIFLocalizationUniProt · AlphaFold · HPA
Whether an antibody against RAD51B can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.34
- Highest tissue expression
- 12 nTPM
Expression across tissuesHPA
Tissue
- salivary gland: 12 nTPM
- epididymis: 8.4 nTPM
- bone marrow: 7 nTPM
- thymus: 5.5 nTPM
- breast: 5.2 nTPM
- ovary: 5.2 nTPM
Single-cell type
- pituitary stem cells: 1,280 nCPM
- renal connecting tubule cells: 936 nCPM
- neutrophil progenitors: 822 nCPM
- renal collecting duct principal cells: 704 nCPM
- ependymal cells: 678 nCPM
- microglia: 611 nCPM
Immune cell
- basophil: 18 nTPM
- memory B-cell: 15 nTPM
- naive B-cell: 13 nTPM
- naive CD4 T-cell: 10 nTPM
- T-reg: 9.7 nTPM
- naive CD8 T-cell: 9.4 nTPM
Brain region
- white matter: 18 nTPM
- choroid plexus: 15 nTPM
- medulla oblongata: 15 nTPM
- basal ganglia: 15 nTPM
- pons: 14 nTPM
- thalamus: 14 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about RAD51B.
Disease | GeneticClinVar
1 pathogenic / likely-pathogenic of 632 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- RAD51B-related cancer predisposition
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.63
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.67
- DepMap mean gene effect
- -0.25
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- blastocyst growth
- DNA recombination
- DNA repair
- double-strand break repair via homologous recombination
- positive regulation of cell population proliferation
- positive regulation of G2/M transition of mitotic cell cycle
- reciprocal meiotic recombination
- somite development
Molecular functions
- ATP binding
- ATP-dependent activity, acting on DNA
- ATP-dependent DNA damage sensor activity
- DNA binding
- double-stranded DNA binding
- single-stranded DNA binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
- AAA+ ATPase domain
- Rad51-like, C-terminal
- DNA recombination and repair protein, RecA-like
- DNA recombination and repair protein RecA-like, ATP-binding domain
- P-loop containing nucleoside triphosphate hydrolase
- XRCC3/RAD51 homolog 2, helix-hairpin-helix domain
- Rad51
- XRCC3/RpoA-like, helix-hairpin-helix domain
- DNA repair protein RAD51 homologue 2
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of RAD51B in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads RAD51B as an antibody target. Whether an autoantibody or antibody against RAD51B could matter depends on whether native RAD51B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
RAD51B is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label RAD51B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...