Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C51004> ?p ?o ?g. }
- NCIT_C51004 IAO_0000115 "Human PRKDC wild-type allele is located in the vicinity of 8q11 and is approximately 187 kb in length. This allele, which encodes PMS1 protein homolog 2 protein, may play a role in DNA double strand break repair and several other processes." @default.
- NCIT_C51004 NCIT_NHC0 "C51004" @default.
- NCIT_C51004 NCIT_P100 "600899" @default.
- NCIT_C51004 NCIT_P102 "NM_006904" @default.
- NCIT_C51004 NCIT_P106 "Gene or Genome" @default.
- NCIT_C51004 NCIT_P107 "PRKDC wt Allele" @default.
- NCIT_C51004 NCIT_P108 "PRKDC wt Allele" @default.
- NCIT_C51004 NCIT_P207 "C1705560" @default.
- NCIT_C51004 NCIT_P211 "DNA recombination" @default.
- NCIT_C51004 NCIT_P211 "double-strand break repair" @default.
- NCIT_C51004 NCIT_P211 "protein kinase activity" @default.
- NCIT_C51004 NCIT_P211 "protein modification" @default.
- NCIT_C51004 NCIT_P321 "5591" @default.
- NCIT_C51004 NCIT_P322 "CTRP" @default.
- NCIT_C51004 NCIT_P366 "PRKDC_wt_Allele" @default.
- NCIT_C51004 NCIT_P96 "DNA-Activated Protein Kinase Catalytic Subunit" @default.
- NCIT_C51004 NCIT_P98 "PRKDC relies on the heterodimer Ku70/Ku80 autoantigen, the DNA-binding DNA-PK component, to direct it to DNA double-stranded breaks for other discontinuities in the DNA double helix and trigger its kinase activity. PRKDC is critical for repair of DNA double strand breaks via the nonhomologous DNA end joining, telomere maintenance via telomere capping, innate immune response via V(D)J recombination (where V is variable, D is diversity, and J is joining) as well as transcriptional regulation via p53, the site-specific recombination process in developing B and T lymphocytes to generate the variable regions of immunoglobulin and T cell receptor genes." @default.
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- NCIT_C51004 hasExactSynonym "DNA-PKcs" @default.
- NCIT_C51004 hasExactSynonym "DNAPK" @default.
- NCIT_C51004 hasExactSynonym "DNPK1" @default.
- NCIT_C51004 hasExactSynonym "HYRC" @default.
- NCIT_C51004 hasExactSynonym "HYRC1" @default.
- NCIT_C51004 hasExactSynonym "Hyper-Radiosensitivity of Murine SCID Mutation, Complementing 1 Gene" @default.
- NCIT_C51004 hasExactSynonym "Hyperradiosensitivity Complementing 1, Mouse, Homolog of Gene" @default.
- NCIT_C51004 hasExactSynonym "IMD26" @default.
- NCIT_C51004 hasExactSynonym "PRKDC wt Allele" @default.
- NCIT_C51004 hasExactSynonym "Protein Kinase, DNA-Activated, Catalytic Polypeptide wt Allele" @default.
- NCIT_C51004 hasExactSynonym "XRCC7" @default.
- NCIT_C51004 hasExactSynonym "p350" @default.
- NCIT_C51004 inSubset NCIT_C116977 @default.
- NCIT_C51004 inSubset NCIT_C142799 @default.
- NCIT_C51004 inSubset NCIT_C142800 @default.
- NCIT_C51004 type Class @default.