About: XRCC5 wt Allele     Goto   Sponge   NotDistinct   Permalink

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AttributesValues
rdf:type
rdfs:label
  • XRCC5 wt Allele
rdfs:subClassOf
OMIM_Number
  • 194364
GenBank_Accession_Number
  • NM_021141
Semantic_Type
  • Gene or Genome
Preferred_Name
  • XRCC5 wt Allele
UMLS_CUI
  • C1710692
GO_Annotation
  • double-stranded DNA bindingGO:0003690TAS29-SEP-2003CGAP
  • DNA recombinationGO:0006310TAS29-SEP-2003CGAP
  • nucleusGO:0005634TAS29-SEP-2003CGAP
  • ATP dependent DNA helicase activityGO:0004003TAS29-SEP-2003CGAP
  • double-strand break repairGO:0006302TAS29-SEP-2003CGAP
EntrezGene_ID
  • 7520
Legacy_Concept_Name
  • XRCC5_wt_Allele
HGNC_ID
  • HGNC:12833
FULL_SYN
  • XRCC5 wt AllelePTNCI
  • Ku80SYNCI
  • G22P2SYNCI
  • Ku Antigen, 80-Kd Subunit GeneSYNCI
  • X-ray Repair Complementing Defective Repair in Chinese Hamster Cells 5 (Double-Strand-Break Rejoining; Ku Autoantigen, 80kDa)wt AlleleSYNCI
Gene_Encodes_Product
  • Ku80 Protein
DEFINITION
  • Human XRCC5 wild-type allele is located within 2q35 and is approximately 99 kb in length. This allele, which encodes ATP-dependent DNA helicase 2 subunit 2 protein, is involved in double-strand break DNA repair and chromosomal translocation. A rare microsatellite polymorphism in this allele is associated with cancer in patients of varying radiosensitivity.NCI
code
  • C50989
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