XRCC2
DNA repair protein XRCC2
Also known as: FANCU, XRCC2_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O43543
- Gene
- XRCC2
- Ensembl
- ENSG00000196584
- Chromosome
- 7
- Canonical length
- 280 aa
- Protein class
- Cancer-related genes, Disease related genes, Human disease related genes, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Vesicles
OverviewNCBI Gene
This gene encodes a member of the RecA/Rad51-related protein family that participates in homologous recombination to maintain chromosome stability and repair DNA damage. This gene is involved in the repair of DNA double-strand breaks by homologous recombination and it functionally complements Chinese hamster irs1, a repair-deficient mutant that exhibits hypersensitivity to a number of different DNA-damaging agents. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
280 residues, UniProt reviewed canonical sequence.
>O43543|XRCC2
1 MCSAFHRAES GTELLARLEG RSSLKEIEPN LFADEDSPVH GDILEFHGPE GTGKTEMLYH
61 LTARCILPKS EGGLEVEVLF IDTDYHFDML RLVTILEHRL SQSSEEIIKY CLGRFFLVYC
121 SSSTHLLLTL YSLESMFCSH PSLCLLILDS LSAFYWIDRV NGGESVNLQE STLRKCSQCL
181 EKLVNDYRLV LFATTQTIMQ KASSSSEEPS HASRRLCDVD IDYRPYLCKA WQQLVKHRMF
241 FSKQDDSQSS NQFSLVSRCL KSNSLKKHFF IIGESGVEFCLocalizationUniProt · AlphaFold · HPA
Whether an antibody against XRCC2 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)
- 0.28
- Highest tissue expression
- 5.5 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 5.5 nTPM
- thymus: 3.6 nTPM
- testis: 3.1 nTPM
- lymph node: 3 nTPM
- tonsil: 2.6 nTPM
- appendix: 2.3 nTPM
Single-cell type
- megakaryocyte progenitors: 102 nCPM
- erythrocyte progenitors: 44 nCPM
- early primary spermatocytes: 42 nCPM
- extravillous trophoblasts: 32 nCPM
- monocyte progenitors: 24 nCPM
- migrating cytotrophoblasts: 23 nCPM
Immune cell
- neutrophil: 0.3 nTPM
- basophil: 0.2 nTPM
- eosinophil: 0.2 nTPM
- gdT-cell: 0.2 nTPM
- memory CD4 T-cell: 0.2 nTPM
- T-reg: 0.2 nTPM
Brain region
- cerebellum: 23 nTPM
- cerebral cortex: 22 nTPM
- white matter: 20 nTPM
- hypothalamus: 18 nTPM
- thalamus: 18 nTPM
- pons: 18 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about XRCC2.
Disease | AllUniProt
Conditions XRCC2 is implicated in, by any mechanism.
- Fanconi anemia, complementation group U (FANCU) MIM:617247
- Spermatogenic failure 50 (SPGF50) MIM:619145
- Premature ovarian failure 17 (POF17) MIM:619146
Disease | GeneticClinVar
17 pathogenic / likely-pathogenic of 839 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Hereditary cancer-predisposing syndrome
- Breast carcinoma
- Fanconi anemia complementation group U
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)
- 1.37
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.13
- DepMap mean gene effect
- -0.42
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 8% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- centrosome cycle
- DNA repair
- DNA strand invasion
- double-strand break repair via homologous recombination
- in utero embryonic development
- meiotic cell cycle
- mitotic cell cycle
- multicellular organism growth
- negative regulation of neuron apoptotic process
- neurogenesis
- positive regulation of neurogenesis
- regulation of fibroblast apoptotic process
- response to gamma radiation
- response to X-ray
- somitogenesis
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of XRCC2 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 XRCC2 as an antibody target. Whether an autoantibody or antibody against XRCC2 could matter depends on whether native XRCC2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
XRCC2 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 XRCC2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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