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- NCIT_C80071 IAO_0000115 "Human RAG2 wild-type allele is located in the vicinity of 11p13 and is approximately 6 kb in length. This allele, which encodes V(D)J recombination-activating protein 2, is involved in the regulation of immunoglobulin recombination. Mutation of the gene is associated with several hereditary immunodeficiencies. Genetic variation may be associated with the relapse of acute lymphoblastic leukemia." @default.
- NCIT_C80071 NCIT_NHC0 "C80071" @default.
- NCIT_C80071 NCIT_P100 "179616" @default.
- NCIT_C80071 NCIT_P102 "AF080577" @default.
- NCIT_C80071 NCIT_P106 "Gene or Genome" @default.
- NCIT_C80071 NCIT_P107 "RAG2 wt Allele" @default.
- NCIT_C80071 NCIT_P108 "RAG2 wt Allele" @default.
- NCIT_C80071 NCIT_P171 "19039135" @default.
- NCIT_C80071 NCIT_P207 "C2698932" @default.
- NCIT_C80071 NCIT_P321 "5897" @default.
- NCIT_C80071 NCIT_P322 "CTRP" @default.
- NCIT_C80071 NCIT_P366 "RAG2_wt_Allele" @default.
- NCIT_C80071 NCIT_P98 "Mutations in the RAG2 gene are associated with combined cellular and humoral immune defects with granulomas, severe combined immunodeficiency, and Omenn syndrome. (UniProt)" @default.
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- NCIT_C80071 normalizedInformationContent "100" @default.
- NCIT_C80071 referenceCount "1" @default.
- NCIT_C80071 hasExactSynonym "RAG-2" @default.
- NCIT_C80071 hasExactSynonym "RAG2 wt Allele" @default.
- NCIT_C80071 hasExactSynonym "Recombination Activating 2 wt Allele" @default.
- NCIT_C80071 hasExactSynonym "Recombination Activating Gene 2 Gene" @default.
- NCIT_C80071 hasExactSynonym "Recombination-Activating Gene 2 Gene" @default.
- NCIT_C80071 hasExactSynonym "V(D)J Recombination-Activating Protein 2 Gene" @default.
- NCIT_C80071 inSubset NCIT_C116977 @default.
- NCIT_C80071 inSubset NCIT_C142799 @default.
- NCIT_C80071 inSubset NCIT_C142800 @default.
- NCIT_C80071 type Class @default.
- NCIT_C80071 isDefinedBy ncit.owl @default.
- NCIT_C80071 label "RAG2 wt Allele" @default.
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