Xrcc2 | ENSMUSG00000028933 | NCBI 57434

Details for: Xrcc2

Gene ID: 57434

Symbol: Xrcc2

Ensembl ID: ENSMUSG00000028933

Description: X-ray repair complementing defective repair in Chinese hamster cells 2

Associated with

Dna double-strand break repair
(R-MMU-5693532)
Hdr through homologous recombination (hrr)
(R-MMU-5685942)
Hdr through homologous recombination (hrr) or single strand annealing (ssa)
(R-MMU-5693567)
Homologous dna pairing and strand exchange
(R-MMU-5693579)
Homology directed repair
(R-MMU-5693538)
Presynaptic phase of homologous dna pairing and strand exchange
(R-MMU-5693616)
Resolution of d-loop structures
(R-MMU-5693537)
Resolution of d-loop structures through holliday junction intermediates
(R-MMU-5693568)
Atp-dependent dna damage sensor activity
(GO:0140664)
Atp binding
(GO:0005524)
Centrosome
(GO:0005813)
Centrosome cycle
(GO:0007098)
Dna binding
(GO:0003677)
Dna damage response
(GO:0006974)
Dna recombination
(GO:0006310)
Dna repair
(GO:0006281)
Dna strand invasion
(GO:0042148)
Double-strand break repair via homologous recombination
(GO:0000724)
Four-way junction dna binding
(GO:0000400)
Intracellular membrane-bounded organelle
(GO:0043231)
In utero embryonic development
(GO:0001701)
Mitotic cell cycle
(GO:0000278)
Multicellular organism growth
(GO:0035264)
Negative regulation of neuron apoptotic process
(GO:0043524)
Neurogenesis
(GO:0022008)
Nucleoplasm
(GO:0005654)
Nucleus
(GO:0005634)
Positive regulation of neurogenesis
(GO:0050769)
Protein binding
(GO:0005515)
Rad51b-rad51c-rad51d-xrcc2 complex
(GO:0033063)
Regulation of fibroblast apoptotic process
(GO:2000269)
Replication fork
(GO:0005657)
Response to gamma radiation
(GO:0010332)
Response to x-ray
(GO:0010165)
Somitogenesis
(GO:0001756)

Other Information

Proteins

DNA repair protein XRCC2

Genular Protein ID: 935070859

Symbol: XRCC2_MOUSE

Name: DNA repair protein XRCC2

UniProtKB Accession Codes:

Q9CX47 O88730 Q9D5T1

Database IDs:

Citations:

PubMed ID: 9628903

Title: The XRCC2 DNA repair gene from human and mouse encodes a novel member of the recA/RAD51 family.

PubMed ID: 9628903

DOI: 10.1093/nar/26.13.3084

PubMed ID: 16141072

Title: The transcriptional landscape of the mammalian genome.

PubMed ID: 16141072

DOI: 10.1126/science.1112014

PubMed ID: 15489334

Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).

PubMed ID: 15489334

DOI: 10.1101/gr.2596504

PubMed ID: 30042186

Title: XRCC2 mutation causes meiotic arrest, azoospermia and infertility.

PubMed ID: 30042186

DOI: 10.1136/jmedgenet-2017-105145

Sequence Information:

Length: 278
Mass: 31391
Checksum: 8E65467596E604FD
Sequence:

MCSDFRRAES GTELLARLEG RSSLKELEPN LFADEDSPVH GDIFEFHGPE GTGKTEMLYH 
LTARCILPKS EGGLQIEVLF IDTDYHFDML RLVTVLEHRL SQSSEEAMKL CLARLFLAYC 
SSSMQLLLTL HSLEALLCSR PSLCLLIVDS LSSFYWIDRV SGGESVALQE STLQKCSQLL 
ERLVTEYRLL LFATTQSLMQ KGSDSADGPS SSKHPCDGDM GYRAYLCKAW QRVVKHRVIF 
SRDDEAKSSR FSLVSRHLKS NSLKKHSFMV RESGVEFC

The gene details are incomplete or unavailable at the moment.

Database document:

This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.

Details for: Xrcc2

Associated with

Other Information

The XRCC2 DNA repair gene from human and mouse encodes a novel member of the recA/RAD51 family. PubMed ID: 9628903

The transcriptional landscape of the mammalian genome. PubMed ID: 16141072

The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). PubMed ID: 15489334

XRCC2 mutation causes meiotic arrest, azoospermia and infertility. PubMed ID: 30042186

Database document:

PubMed ID: 9628903

PubMed ID: 16141072

PubMed ID: 15489334

PubMed ID: 30042186