BRCA2 · P51587
In brief
BRCA2 is UniProt protein record P51587 for Homo sapiens (NCBI 9606). The retained sequence contains 3418 amino acids. [1]
Evidence for this statement
Source annotation
Where to check this statement
- uniprot-P51587
- Captured UniProt JSON: primaryAccession, organism, sequence and FUNCTION comments
Save, investigate and check this version
Editorial draft · human review pending
Ask about this materialOn this page
Meet the protein
BRCA2 helps preserve genome integrity. UniProt describes its main role in homologous recombination, a process that repairs damaged DNA using a similar sequence. BRCA2 helps place RAD51 on single-stranded DNA at a damaged region. RAD51 performs strand exchange; BRCA2 helps establish the conditions in which RAD51 can work.
[1]Evidence for this statement
Editorial synthesis
Where to check this statement
- uniprot-P51587
- Captured UniProt JSON: primaryAccession, organism, sequence and FUNCTION comments
DNA repair involves several interacting proteins. UniProt describes BRCA2 helping assemble and stabilize RAD51 on DNA and connects individual statements to publications. Compare this explanation with the original annotation, evidence codes and sequence below. These data describe the selected human entry P51587; they do not automatically establish the function of every sequence variant.
[1]Evidence for this statement
Editorial synthesis
Where to check this statement
- uniprot-P51587
- Captured UniProt JSON: primaryAccession, organism, sequence and FUNCTION comments
Repair depends on organised strand exchange
After a DNA break, a damaged region must be connected with a suitable homologous sequence. BRCA2 helps assemble RAD51 on single-stranded DNA and stabilise the resulting filament; RAD51 then carries out strand exchange. The retained UniProt annotation also links BRCA2 to replication-associated and meiotic contexts. This is why one protein can connect different genome-maintenance questions. Its full sequence, interacting partners and the evidence for each function provide complementary information.
[1]Evidence for this statement
EcoGenesis
Where to check this statement
- uniprot-P51587
- Retained UniProt JSON: comments[commentType=FUNCTION], selected accession and entry version as recorded in evidence
Teaching diagram
Evidence for this statement
EcoGenesis
Damaged DNA
The repair substrate
BRCA2 and RAD51
Assembly and stabilisation
Strand exchange
RAD51-mediated step
- Damaged DNA → BRCA2 and RAD51: connects with
- BRCA2 and RAD51 → Strand exchange: connects with
What is known about function
Function and evidence from UniProt
Inspect structured data
- Source text
- Tumor suppressor protein that maintains genome stability primarily by repairing damaged DNA through homologous recombination (HR) (PubMed:11239456, PubMed:12442171, PubMed:15115758, PubMed:15199141, PubMed:15671039, PubMed:15937124, PubMed:17515903, PubMed:17515904, PubMed:18317453, PubMed:19303847, PubMed:20729832, PubMed:20729858, PubMed:20729859, PubMed:21719596, PubMed:27941124, PubMed:37499663, PubMed:37515771). Facilitates the repair of double-strand breaks (DSBs) by binding and mediating the loading of the RAD51 protein onto single-stranded DNA (ssDNA), thereby promoting the activity of RAD51, which catalyzes DNA strand exchange (PubMed:11239456, PubMed:12442171, PubMed:15937124, PubMed:17515903, PubMed:17515904, PubMed:18317453, PubMed:19303847, PubMed:20729832, PubMed:20729858, PubMed:20729859, PubMed:27941124, PubMed:37499663). BRCA2 nucleates and stabilizes RAD51 on ssDNA directly and delivers RAD51 to ssDNA-double-stranded DNA (dsDNA) junctions by sliding along dsDNA backbone (PubMed:12442171, PubMed:19303847, PubMed:37499663). RAD51 targeting to ssDNA promotes removal of replication protein-A (RPA) from ssDNA and stabilization of RAD51-ssDNA filaments by blocking ATP hydrolysis (PubMed:20729859). May play a role in the extension step after strand invasion at replication-dependent DNA double-strand breaks; together with PALB2 is involved in both POLH localization at collapsed replication forks and DNA polymerization activity (PubMed:24485656). Required to prevent R-loop-associated DNA damage and thus transcription-associated genomic instability (PubMed:24896180). Silencing of BRCA2 promotes R-loop accumulation at actively transcribed genes in replicating and non-replicating cells, suggesting that BRCA2 mediates the control of R-loop associated genomic instability, independently of its known role in homologous recombination (PubMed:24896180). Also promotes RAD51 loading to telomeric regions, facilitating telomere replication and capping (PubMed:21076401). Also required for homologous recombination during meiosis by promoting the recruitment of RAD51 and DMC1 recombinases to meiotic DSB sites, enabling proper chromosome pairing and crossing over (PubMed:26976601). Also promotes homologous recombination by inactivating the FIGNL1-FIRRM complex to protect RAD51 filament from premature disassembly (PubMed:37515771). Together with NPM1, may also regulate centrosome duplication (PubMed:21084279)
- Source language
- en
- evidence codes
- evidenceCode
- ECO:0000269
- Source
- PubMed
- id
- 11239456
- evidenceCode
- ECO:0000269
- Source
- PubMed
- id
- 12442171
- evidenceCode
- ECO:0000269
- Source
- PubMed
- id
- 15115758
- evidenceCode
- ECO:0000269
- Source
- PubMed
- id
- 15199141
- evidenceCode
- ECO:0000269
- Source
- PubMed
- id
- 15671039
- evidenceCode
- ECO:0000269
- Source
- PubMed
- id
- 15937124
- evidenceCode
- ECO:0000269
- Source
- PubMed
- id
- 17515903
- evidenceCode
- ECO:0000269
- Source
- PubMed
- id
- 17515904
- evidenceCode
- ECO:0000269
- Source
- PubMed
- id
- 18317453
- evidenceCode
- ECO:0000269
- Source
- PubMed
- id
- 19303847
- evidenceCode
- ECO:0000269
- Source
- PubMed
- id
- 20729832
- evidenceCode
- ECO:0000269
- Source
- PubMed
- id
- 20729858
- evidenceCode
- ECO:0000269
- Source
- PubMed
- id
- 20729859
- evidenceCode
- ECO:0000269
- Source
- PubMed
- id
- 21076401
- evidenceCode
- ECO:0000269
- Source
- PubMed
- id
- 21084279
- evidenceCode
- ECO:0000269
- Source
- PubMed
- id
- 21719596
- evidenceCode
- ECO:0000269
- Source
- PubMed
- id
- 24485656
- evidenceCode
- ECO:0000269
- Source
- PubMed
- id
- 24896180
- evidenceCode
- ECO:0000269
- Source
- PubMed
- id
- 26976601
- evidenceCode
- ECO:0000269
- Source
- PubMed
- id
- 27941124
- evidenceCode
- ECO:0000269
- Source
- PubMed
- id
- 37499663
- evidenceCode
- ECO:0000269
- Source
- PubMed
- id
- 37515771
Evidence for this statement
Source annotation
Where to check this statement
- uniprot-P51587
- Captured UniProt JSON: comments[commentType=FUNCTION] and attached evidence codes
Evidence codes qualify the annotation. This record is not a measurement of an illustrated specimen.
Sequence and version
P51587
Inspect structured data
- accession
- P51587
- name
- Breast cancer type 2 susceptibility protein
- length
- 3418
- entry version
- 252
- sequence version
- 4
- Sequence
MPIGSKERPTFFEIFKTRCNKADLGPISLNWFEELSSEAPPYNSEPAEESEHKNNNYEPN LFKTPQRKPSYNQLASTPIIFKEQGLTLPLYQSPVKELDKFKLDLGRNVPNSRHKSLRTV KTKMDQADDVSCPLLNSCLSESPVVLQCTHVTPQRDKSVVCGSLFHTPKFVKGRQTPKHI SESLGAEVDPDMSWSSSLATPPTLSSTVLIVRNEEASETVFPHDTTANVKSYFSNHDESL KKNDRFIASVTDSENTNQREAASHGFGKTSGNSFKVNSCKDHIGKSMPNVLEDEVYETVV DTSEEDSFSLCFSKCRTKNLQKVRTSKTRKKIFHEANADECEKSKNQVKEKYSFVSEVEP NDTDPLDSNVANQKPFESGSDKISKEVVPSLACEWSQLTLSGLNGAQMEKIPLLHISSCD QNISEKDLLDTENKRKKDFLTSENSLPRISSLPKSEKPLNEETVVNKRDEEQHLESHTDC ILAVKQAISGTSPVASSFQGIKKSIFRIRESPKETFNASFSGHMTDPNFKKETEASESGL EIHTVCSQKEDSLCPNLIDNGSWPATTTQNSVALKNAGLISTLKKKTNKFIYAIHDETSY KGKKIPKDQKSELINCSAQFEANAFEAPLTFANADSGLLHSSVKRSCSQNDSEEPTLSLT SSFGTILRKCSRNETCSNNTVISQDLDYKEAKCNKEKLQLFITPEADSLSCLQEGQCEND PKSKKVSDIKEEVLAAACHPVQHSKVEYSDTDFQSQKSLLYDHENASTLILTPTSKDVLS NLVMISRGKESYKMSDKLKGNNYESDVELTKNIPMEKNQDVCALNENYKNVELLPPEKYM RVASPSRKVQFNQNTNLRVIQKNQEETTSISKITVNPDSEELFSDNENNFVFQVANERNN LALGNTKELHETDLTCVNEPIFKNSTMVLYGDTGDKQATQVSIKKDLVYVLAEENKNSVK QHIKMTLGQDLKSDISLNIDKIPEKNNDYMNKWAGLLGPISNHSFGGSFRTASNKEIKLS EHNIKKSKMFFKDIEEQYPTSLACVEIVNTLALDNQKKLSKPQSINTVSAHLQSSVVVSD CKNSHITPQMLFSKQDFNSNHNLTPSQKAEITELSTILEESGSQFEFTQFRKPSYILQKS TFEVPENQMTILKTTSEECRDADLHVIMNAPSIGQVDSSKQFEGTVEIKRKFAGLLKNDC NKSASGYLTDENEVGFRGFYSAHGTKLNVSTEALQKAVKLFSDIENISEETSAEVHPISL SSSKCHDSVVSMFKIENHNDKTVSEKNNKCQLILQNNIEMTTGTFVEEITENYKRNTENE DNKYTAASRNSHNLEFDGSDSSKNDTVCIHKDETDLLFTDQHNICLKLSGQFMKEGNTQI KEDLSDLTFLEVAKAQEACHGNTSNKEQLTATKTEQNIKDFETSDTFFQTASGKNISVAK ESFNKIVNFFDQKPEELHNFSLNSELHSDIRKNKMDILSYEETDIVKHKILKESVPVGTG NQLVTFQGQPERDEKIKEPTLLGFHTASGKKVKIAKESLDKVKNLFDEKEQGTSEITSFS HQWAKTLKYREACKDLELACETIEITAAPKCKEMQNSLNNDKNLVSIETVVPPKLLSDNL CRQTENLKTSKSIFLKVKVHENVEKETAKSPATCYTNQSPYSVIENSALAFYTSCSRKTS VSQTSLLEAKKWLREGIFDGQPERINTADYVGNYLYENNSNSTIAENDKNHLSEKQDTYL SNSSMSNSYSYHSDEVYNDSGYLSKNKLDSGIEPVLKNVEDQKNTSFSKVISNVKDANAY PQTVNEDICVEELVTSSSPCKNKNAAIKLSISNSNNFEVGPPAFRIASGKIVCVSHETIK KVKDIFTDSFSKVIKENNENKSKICQTKIMAGCYEALDDSEDILHNSLDNDECSTHSHKV FADIQSEEILQHNQNMSGLEKVSKISPCDVSLETSDICKCSIGKLHKSVSSANTCGIFST ASGKSVQVSDASLQNARQVFSEIEDSTKQVFSKVLFKSNEHSDQLTREENTAIRTPEHLI SQKGFSYNVVNSSAFSGFSTASGKQVSILESSLHKVKGVLEEFDLIRTEHSLHYSPTSRQ NVSKILPRVDKRNPEHCVNSEMEKTCSKEFKLSNNLNVEGGSSENNHSIKVSPYLSQFQQ DKQQLVLGTKVSLVENIHVLGKEQASPKNVKMEIGKTETFSDVPVKTNIEVCSTYSKDSE NYFETEAVEIAKAFMEDDELTDSKLPSHATHSLFTCPENEEMVLSNSRIGKRRGEPLILV GEPSIKRNLLNEFDRIIENQEKSLKASKSTPDGTIKDRRLFMHHVSLEPITCVPFRTTKE RQEIQNPNFTAPGQEFLSKSHLYEHLTLEKSSSNLAVSGHPFYQVSATRNEKMRHLITTG RPTKVFVPPFKTKSHFHRVEQCVRNINLEENRQKQNIDGHGSDDSKNKINDNEIHQFNKN NSNQAVAVTFTKCEEEPLDLITSLQNARDIQDMRIKKKQRQRVFPQPGSLYLAKTSTLPR ISLKAAVGGQVPSACSHKQLYTYGVSKHCIKINSKNAESFQFHTEDYFGKESLWTGKGIQ LADGGWLIPSNDGKAGKEEFYRALCDTPGVDPKLISRIWVYNHYRWIIWKLAAMECAFPK EFANRCLSPERVLLQLKYRYDTEIDRSRRSAIKKIMERDDTAAKTLVLCVSDIISLSANI SETSSNKTSSADTQKVAIIELTDGWYAVKAQLDPPLLAVLKNGRLTVGQKIILHGAELVG SPDACTPLEAPESLMLKISANSTRPARWYTKLGFFPDPRPFPLPLSSLFSDGGNVGCVDV IIQRAYPIQWMEKTSSGLYIFRNEREEEKEAAKYVEAQQKRLEALFTKIQEEFEEHEENT TKPYLPSRALTRQQVRALQDGAELYEAVKNAADPAYLEGYFSEEQLRALNNHRQMLNDKK QAQIQLEIRKAMESAEQKEQGLSRDVTTVWKLRIVSYSKKEKDSVILSIWRPSSDLYSLL TEGKRYRIYHLATSKSKSKSERANIQLAATKKTQYQQLPVSDEILFQIYQPREPLHFSKF LDPDFQPSCSEVDLIGFVVSVVKKTGLAPFVYLSDECYNLLAIKFWIDLNEDIIKPHMLI AASNLQWRPESKSGLLTLFAGDFSVFSASPKEGHFQETFNKMKNTVENIDILCNEAENKL MHILHANDPKWSTPTKDCTSGPYTAQIIPGTGNKLLMSSPNCEIYYQSPLSLCMAKRKSV STPVSAQMTSKSCKGEKEIDDQKNCKKRRALDFLSRLPLPPPVSPICTFVSPAAQKAFQP PRSCGTKYETPIKKKELNSPQMTPFKKFNEISLLESNSIADEELALINTQALLSGSTGEK QFISVSESTRTAPTSSEDYLRLKRRCTTSLIKEQESSQASTEECEKNKQDTITTKKYI
Evidence for this statement
Source annotation
Where to check this statement
- uniprot-P51587
- Captured UniProt JSON: sequence.value, sequence.length, sequenceVersion and entryVersion
Genes and domains
Cross-references supplied by UniProt
Inspect structured data
- gene symbols
- BRCA2
- gene crossreferences
- database
- Ensembl
- id
- ENST00000380152.8
- properties
- key
- ProteinId
- value
- ENSP00000369497.3
- key
- GeneId
- value
- ENSG00000139618.19
- database
- Ensembl
- id
- ENST00000544455.6
- properties
- key
- ProteinId
- value
- ENSP00000439902.1
- key
- GeneId
- value
- ENSG00000139618.19
- database
- Ensembl
- id
- ENST00000680887.1
- properties
- key
- ProteinId
- value
- ENSP00000505508.1
- key
- GeneId
- value
- ENSG00000139618.19
- database
- GeneID
- id
- 675
- properties
- key
- Description
- value
- -
- interpro domains
- Provider
- interpro
- accession
- IPR015525
- name
- BRCA2
- Provider
- interpro
- accession
- IPR015252
- name
- BRCA2_hlx
- Provider
- interpro
- accession
- IPR036315
- name
- BRCA2_hlx_sf
- Provider
- interpro
- accession
- IPR015187
- name
- BRCA2_OB_1
- Provider
- interpro
- accession
- IPR048262
- name
- BRCA2_OB_2_dom
- Provider
- interpro
- accession
- IPR015188
- name
- BRCA2_OB_3
- Provider
- interpro
- accession
- IPR002093
- name
- BRCA2_repeat
- Provider
- interpro
- accession
- IPR055077
- name
- BRCA2_TR2
- Provider
- interpro
- accession
- IPR012340
- name
- NA-bd_OB-fold
- Provider
- interpro
- accession
- IPR015205
- name
- Tower_dom
Evidence for this statement
Source annotation
Where to check this statement
- uniprot-P51587
- Captured UniProt JSON: genes, features and cross-references
GO function annotations
A sample with evidence codes
Inspect structured data
Shown / materialized / in provider response: 12 / 169 / 169
| GO | Evidence | Publication or rule | Assigned by |
|---|---|---|---|
| GO:0004402 histone acetyltransferase activity Molecular Function | ECO:0000314 NOT|enables | PMID:9824164 | UniProt 20060718 |
| GO:0002020 protease binding Molecular Function | ECO:0000353 enables | PMID:15314155 | UniProt 20100604 |
| GO:0003690 double-stranded DNA binding Molecular Function | ECO:0000314 enables | PMID:37499663 | UniProt 20260302 |
| GO:0003697 single-stranded DNA binding Molecular Function | ECO:0000318 enables | GO_REF:0000033 | GO_Central 20250320 |
| GO:0003697 single-stranded DNA binding Molecular Function | ECO:0000314 enables | PMID:20729832 | UniProt 20101006 |
| GO:0003697 single-stranded DNA binding Molecular Function | ECO:0000314 enables | PMID:37499663 | UniProt 20260302 |
| GO:0005515 protein binding Molecular Function | ECO:0000353 enables | PMID:10373512 | UniProt 20070807 |
| GO:0005515 protein binding Molecular Function | ECO:0000353 enables | PMID:10373512 | IntAct 20260725 |
| GO:0005515 protein binding Molecular Function | ECO:0000353 enables | PMID:10551859 | IntAct 20260725 |
| GO:0005515 protein binding Molecular Function | ECO:0000353 enables | PMID:11597317 | UniProt 20070807 |
| GO:0005515 protein binding Molecular Function | ECO:0000353 enables | PMID:12242698 | UniProt 20090624 |
| GO:0005515 protein binding Molecular Function | ECO:0000353 enables | PMID:12242698 | UniProt 20070807 |
Evidence for this statement
Source annotation
- Gene Ontology Consortium / QuickGO · UniProtKB:P51587
- Gene Ontology Consortium / QuickGO · UniProtKB:P51587
Where to check this statement
- quickgo-P51587-1
- Captured QuickGO annotation results: GO ID, qualifier, evidenceCode, reference, assignedBy and date; limited returned pages
- quickgo-P51587-2
- Captured QuickGO annotation results: GO ID, qualifier, evidenceCode, reference, assignedBy and date; limited returned pages
These are source annotations, not independent proof of a causal mechanism. The complete captured responses are available as originals.
Research cited by the protein record
Bibliographic records
Inspect structured data
- Source
- uniprot
- id
- P51587-citation-8524414
- title
- Identification of the breast cancer susceptibility gene BRCA2.
- pmid
- 8524414
- doi
- 10.1038/378789a0
- year
- 1995
- authors
- Wooster R.
- Bignell G.
- Lancaster J.
- Swift S.
- Seal S.
- Mangion J.
- Collins N.
- Gregory S.
- Gumbs C.
- Micklem G.
- Barfoot R.
- Hamoudi R.
- Patel S.
- Rice C.
- Biggs P.
- Hashim Y.
- Smith A.
- Connor F.
- Arason A.
- Gudmundsson J.
- Ficenec D.
- Kelsell D.
- Ford D.
- Tonin P.
- Bishop D.T.
- Spurr N.K.
- Ponder B.A.J.
- Eeles R.
- Peto J.
- Devilee P.
- Cornelisse C.
- Lynch H.
- Narod S.
- Lenoir G.
- Egilsson V.
- Barkadottir R.B.
- Easton D.F.
- Bentley D.R.
- Futreal P.A.
- Ashworth A.
- Stratton M.R.
- journal
- Nature
- Reuse status
- metadata_only
- Source URL
- https://rest.uniprot.org/uniprotkb/P51587.json
- Source snapshot SHA-256
- befba0a62b75b4f67c7651d0bb175a4ec3ef6a9751be6575af593c9e94cfd82f
- Source
- uniprot
- id
- P51587-citation-8589730
- title
- The complete BRCA2 gene and mutations in chromosome 13q-linked kindreds.
- pmid
- 8589730
- doi
- 10.1038/ng0396-333
- year
- 1996
- authors
- Tavtigian S.V.
- Simard J.
- Rommens J.
- Couch F.
- Shattuck-Eidens D.
- Neuhausen S.
- Merajver S.
- Thorlacius S.
- Offit K.
- Stoppa-Lyonnet D.
- Belanger C.
- Bell R.
- Berry S.
- Bogden R.
- Chen Q.
- Davis T.
- Dumont M.
- Frye C.
- Hattier T.
- Jammulapati S.
- Janecki T.
- Jiang P.
- Kehrer R.
- Leblanc J.-F.
- Mitchell J.T.
- McArthur-Morrison J.
- Nguyen K.
- Peng Y.
- Samson C.
- Schroeder M.
- Snyder S.C.
- Steele L.
- Stringfellow M.
- Stroup C.
- Swedlund B.
- Swensen J.
- Teng D.
- Thomas A.
- Tran T.
- Tran T.
- Tranchant M.
- Weaver-Feldhaus J.
- Wong A.K.C.
- Shizuya H.
- Eyfjord J.E.
- Cannon-Albright L.
- Labrie F.
- Skolnick M.H.
- Weber B.
- Kamb A.
- Goldar D.E.
- journal
- Nat. Genet.
- Reuse status
- metadata_only
- Source URL
- https://rest.uniprot.org/uniprotkb/P51587.json
- Source snapshot SHA-256
- befba0a62b75b4f67c7651d0bb175a4ec3ef6a9751be6575af593c9e94cfd82f
- Source
- uniprot
- id
- P51587-citation-15057823
- title
- The DNA sequence and analysis of human chromosome 13.
- pmid
- 15057823
- doi
- 10.1038/nature02379
- year
- 2004
- authors
- Dunham A.
- Matthews L.H.
- Burton J.
- Ashurst J.L.
- Howe K.L.
- Ashcroft K.J.
- Beare D.M.
- Burford D.C.
- Hunt S.E.
- Griffiths-Jones S.
- Jones M.C.
- Keenan S.J.
- Oliver K.
- Scott C.E.
- Ainscough R.
- Almeida J.P.
- Ambrose K.D.
- Andrews D.T.
- Ashwell R.I.S.
- Babbage A.K.
- Bagguley C.L.
- Bailey J.
- Bannerjee R.
- Barlow K.F.
- Bates K.
- Beasley H.
- Bird C.P.
- Bray-Allen S.
- Brown A.J.
- Brown J.Y.
- Burrill W.
- Carder C.
- Carter N.P.
- Chapman J.C.
- Clamp M.E.
- Clark S.Y.
- Clarke G.
- Clee C.M.
- Clegg S.C.
- Cobley V.
- Collins J.E.
- Corby N.
- Coville G.J.
- Deloukas P.
- Dhami P.
- Dunham I.
- Dunn M.
- Earthrowl M.E.
- Ellington A.G.
- Faulkner L.
- Frankish A.G.
- Frankland J.
- French L.
- Garner P.
- Garnett J.
- Gilbert J.G.R.
- Gilson C.J.
- Ghori J.
- Grafham D.V.
- Gribble S.M.
- Griffiths C.
- Hall R.E.
- Hammond S.
- Harley J.L.
- Hart E.A.
- Heath P.D.
- Howden P.J.
- Huckle E.J.
- Hunt P.J.
- Hunt A.R.
- Johnson C.
- Johnson D.
- Kay M.
- Kimberley A.M.
- King A.
- Laird G.K.
- Langford C.J.
- Lawlor S.
- Leongamornlert D.A.
- Lloyd D.M.
- Lloyd C.
- Loveland J.E.
- Lovell J.
- Martin S.
- Mashreghi-Mohammadi M.
- McLaren S.J.
- McMurray A.
- Milne S.
- Moore M.J.F.
- Nickerson T.
- Palmer S.A.
- Pearce A.V.
- Peck A.I.
- Pelan S.
- Phillimore B.
- Porter K.M.
- Rice C.M.
- Searle S.
- Sehra H.K.
- Shownkeen R.
- Skuce C.D.
- Smith M.
- Steward C.A.
- Sycamore N.
- Tester J.
- Thomas D.W.
- Tracey A.
- Tromans A.
- Tubby B.
- Wall M.
- Wallis J.M.
- West A.P.
- Whitehead S.L.
- Willey D.L.
- Wilming L.
- Wray P.W.
- Wright M.W.
- Young L.
- Coulson A.
- Durbin R.M.
- Hubbard T.
- Sulston J.E.
- Beck S.
- Bentley D.R.
- Rogers J.
- Ross M.T.
- journal
- Nature
- Reuse status
- metadata_only
- Source URL
- https://rest.uniprot.org/uniprotkb/P51587.json
- Source snapshot SHA-256
- befba0a62b75b4f67c7651d0bb175a4ec3ef6a9751be6575af593c9e94cfd82f
- Source
- uniprot
- id
- P51587-citation-7658781
- title
- Linkage to BRCA2 region in hereditary male breast cancer.
- pmid
- 7658781
- doi
- 10.1016/s0140-6736(95)91383-1
- year
- 1995
- authors
- Thorlacius S.
- Tryggvadottir L.
- Olafsdottir G.H.
- Jonasson J.G.
- Ogmundsdottir H.M.
- Tulinius H.
- Eyfjord J.E.
- journal
- Lancet
- Reuse status
- metadata_only
- Source URL
- https://rest.uniprot.org/uniprotkb/P51587.json
- Source snapshot SHA-256
- befba0a62b75b4f67c7651d0bb175a4ec3ef6a9751be6575af593c9e94cfd82f
- Source
- uniprot
- id
- P51587-citation-9150155
- title
- Study of a single BRCA2 mutation with high carrier frequency in a small population.
- pmid
- 9150155
- doi
- —
- year
- 1997
- authors
- Thorlacius S.
- Sigurdsson S.
- Bjarnadottir H.
- Olafsdottir G.
- Jonasson J.G.
- Tryggvadottir L.
- Tulinius H.
- Eyfjoerd J.E.
- journal
- Am. J. Hum. Genet.
- Reuse status
- metadata_only
- Source URL
- https://rest.uniprot.org/uniprotkb/P51587.json
- Source snapshot SHA-256
- befba0a62b75b4f67c7651d0bb175a4ec3ef6a9751be6575af593c9e94cfd82f
- Source
- uniprot
- id
- P51587-citation-9140390
- title
- Germline BRCA2 6174delT mutations in Ashkenazi Jewish pancreatic cancer patients.
- pmid
- 9140390
- doi
- 10.1038/ng0597-17
- year
- 1997
- authors
- Ozcelik H.
- Schmocker B.
- Di Nicola N.
- Shi X.H.
- Langer B.
- Moore M.
- Taylor B.R.
- Narod S.A.
- Darlington G.
- Andrulis I.L.
- Gallinger S.
- Redston M.
- journal
- Nat. Genet.
- Reuse status
- metadata_only
- Source URL
- https://rest.uniprot.org/uniprotkb/P51587.json
- Source snapshot SHA-256
- befba0a62b75b4f67c7651d0bb175a4ec3ef6a9751be6575af593c9e94cfd82f
- Source
- uniprot
- id
- P51587-citation-10584720
- title
- Pregnancy and risk of early breast cancer in carriers of BRCA1 and BRCA2.
- pmid
- 10584720
- doi
- 10.1016/s0140-6736(99)04336-6
- year
- 1999
- authors
- Jernstroem H.
- Lerman C.
- Ghadirian P.
- Lynch H.T.
- Weber B.
- Garber J.
- Daly M.
- Olopade O.I.
- Foulkes W.D.
- Warner E.
- Brunet J.S.
- Narod S.A.
- journal
- Lancet
- Reuse status
- metadata_only
- Source URL
- https://rest.uniprot.org/uniprotkb/P51587.json
- Source snapshot SHA-256
- befba0a62b75b4f67c7651d0bb175a4ec3ef6a9751be6575af593c9e94cfd82f
- Source
- uniprot
- id
- P51587-citation-10373512
- title
- Interaction between the product of the breast cancer susceptibility gene BRCA2 and DSS1, a protein functionally conserved from yeast to mammals.
- pmid
- 10373512
- doi
- 10.1128/mcb.19.7.4633
- year
- 1999
- authors
- Marston N.J.
- Richards W.J.
- Hughes D.
- Bertwistle D.
- Marshall C.J.
- Ashworth A.
- journal
- Mol. Cell. Biol.
- Reuse status
- metadata_only
- Source URL
- https://rest.uniprot.org/uniprotkb/P51587.json
- Source snapshot SHA-256
- befba0a62b75b4f67c7651d0bb175a4ec3ef6a9751be6575af593c9e94cfd82f
- Source
- uniprot
- id
- P51587-citation-11158174
- title
- De novo recurrent germline mutation of the BRCA2 gene in a patient with early onset breast cancer.
- pmid
- 11158174
- doi
- 10.1136/jmg.38.2.102
- year
- 2001
- authors
- van der Luijt R.B.
- van Zon P.H.
- Jansen R.P.
- van der Sijs-Bos C.J.
- Warlam-Rodenhuis C.C.
- Ausems M.G.
- journal
- J. Med. Genet.
- Reuse status
- metadata_only
- Source URL
- https://rest.uniprot.org/uniprotkb/P51587.json
- Source snapshot SHA-256
- befba0a62b75b4f67c7651d0bb175a4ec3ef6a9751be6575af593c9e94cfd82f
- Source
- uniprot
- id
- P51587-citation-11239456
- title
- Role of BRCA2 in control of the RAD51 recombination and DNA repair protein.
- pmid
- 11239456
- doi
- 10.1016/s1097-2765(01)00175-7
- year
- 2001
- authors
- Davies A.A.
- Masson J.Y.
- McIlwraith M.J.
- Stasiak A.Z.
- Stasiak A.
- Venkitaraman A.R.
- West S.C.
- journal
- Mol. Cell
- Reuse status
- metadata_only
- Source URL
- https://rest.uniprot.org/uniprotkb/P51587.json
- Source snapshot SHA-256
- befba0a62b75b4f67c7651d0bb175a4ec3ef6a9751be6575af593c9e94cfd82f
- Source
- uniprot
- id
- P51587-citation-15115758
- title
- Direct interaction of FANCD2 with BRCA2 in DNA damage response pathways.
- pmid
- 15115758
- doi
- 10.1093/hmg/ddh135
- year
- 2004
- authors
- Hussain S.
- Wilson J.B.
- Medhurst A.L.
- Hejna J.
- Witt E.
- Ananth S.
- Davies A.
- Masson J.-Y.
- Moses R.
- West S.C.
- de Winter J.P.
- Ashworth A.
- Jones N.J.
- Mathew C.G.
- journal
- Hum. Mol. Genet.
- Reuse status
- metadata_only
- Source URL
- https://rest.uniprot.org/uniprotkb/P51587.json
- Source snapshot SHA-256
- befba0a62b75b4f67c7651d0bb175a4ec3ef6a9751be6575af593c9e94cfd82f
- Source
- uniprot
- id
- P51587-citation-15199141
- title
- Functional interaction of monoubiquitinated FANCD2 and BRCA2/FANCD1 in chromatin.
- pmid
- 15199141
- doi
- 10.1128/mcb.24.13.5850-5862.2004
- year
- 2004
- authors
- Wang X.Z.
- Andreassen P.R.
- D'Andrea A.D.
- journal
- Mol. Cell. Biol.
- Reuse status
- metadata_only
- Source URL
- https://rest.uniprot.org/uniprotkb/P51587.json
- Source snapshot SHA-256
- befba0a62b75b4f67c7651d0bb175a4ec3ef6a9751be6575af593c9e94cfd82f
Evidence for this statement
Source annotation
Where to check this statement
- uniprot-P51587
- Captured UniProt JSON: references and citation cross-references
Only metadata is shown. Article text has a separate reuse decision.
How to read these records
Organism in the UniProt record
Homo sapiens · NCBI 9606Scientific profile →Your research question
Save the article to return to your question and this source version.
Plan a test
This is your research plan. Completing these fields does not confirm a hypothesis.
Sources and versions
Editorial draft · human review pending
- UniProt Consortium · P51587
2026-09-09T03:19:37.686498+00:00 · CC-BY-4.0
Provenance and original
- Source version
- entry 252; sequence 4
- Original SHA-256
- befba0a62b75b4f67c7651d0bb175a4ec3ef6a9751be6575af593c9e94cfd82f
- Processing
- Unmodified provider response; selected fields are projected into the document.
- Version details
- Native entry and sequence versions retained.
- Gene Ontology Consortium / QuickGO · UniProtKB:P51587
2026-09-09T03:19:39.004762+00:00 · CC-BY-4.0
Provenance and original
- Original SHA-256
- 362e66f46f82c372fb8fc92bb3842b46320fbae8eae85d9497bd550ae9211404
- Processing
- Unmodified provider response; selected fields are projected into the document.
- Version details
- No native GO release was supplied; exact response hash and retrieval time are retained.
- Gene Ontology Consortium / QuickGO · UniProtKB:P51587
2026-09-09T03:19:40.324061+00:00 · CC-BY-4.0
Provenance and original
- Original SHA-256
- f4d7f8c2a54ea95b803629bb8d105b0794cf2d6d68e14ac4e03e501eebeb0594
- Processing
- Unmodified provider response; selected fields are projected into the document.
- Version details
- No native GO release was supplied; exact response hash and retrieval time are retained.
Inspect structured data
- Content version
- 86ac29c9a8dddf1e8aad8c3beab615ec170a2602396a249b7e751c6ea93570d2
- Source version
- research-20260909.1
- Updated
- 2026-10-01