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- NCIT_C106636 IAO_0000115 "Human SETBP1 wild-type allele is located in the vicinity of 18q21.1 and is approximately 388 kb in length. This allele, which encodes SET-binding protein, may play a role in the regulation of protein SET activity. Mutation of the gene is associated with Schinzel-Giedion midface retraction syndrome. A chromosomal translocation, t(11;18)(p15;q12), involving this gene and the NUP98 gene is involved in T-cell acute lymphoblastic leukemia." @default.
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- NCIT_C106636 NCIT_P106 "Gene or Genome" @default.
- NCIT_C106636 NCIT_P107 "SETBP1 wt Allele" @default.
- NCIT_C106636 NCIT_P108 "SETBP1 wt Allele" @default.
- NCIT_C106636 NCIT_P207 "C3815268" @default.
- NCIT_C106636 NCIT_P321 "26040" @default.
- NCIT_C106636 NCIT_P322 "CTRP" @default.
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- NCIT_C106636 hasExactSynonym "KIAA0437" @default.
- NCIT_C106636 hasExactSynonym "MRD29" @default.
- NCIT_C106636 hasExactSynonym "SEB" @default.
- NCIT_C106636 hasExactSynonym "SET Binding Protein 1 wt Allele" @default.
- NCIT_C106636 hasExactSynonym "SETBP1 wt Allele" @default.
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- NCIT_C106636 type Class @default.
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- NCIT_C106636 label "SETBP1 wt Allele" @default.
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