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- NCIT_C75508 IAO_0000115 "Human HIRA wild-type allele is located in the vicinity of 22q11.2 or 22q11.21 and is approximately 101 kb in length. This allele, which encodes protein HIRA, is involved in the modulation of chromatin structure. Haploinsufficiency of the gene may be a factor in DiGeorge syndrome." @default.
- NCIT_C75508 NCIT_NHC0 "C75508" @default.
- NCIT_C75508 NCIT_P100 "600237" @default.
- NCIT_C75508 NCIT_P102 "X75296" @default.
- NCIT_C75508 NCIT_P106 "Gene or Genome" @default.
- NCIT_C75508 NCIT_P107 "HIRA wt Allele" @default.
- NCIT_C75508 NCIT_P108 "HIRA wt Allele" @default.
- NCIT_C75508 NCIT_P207 "C2697539" @default.
- NCIT_C75508 NCIT_P321 "7290" @default.
- NCIT_C75508 NCIT_P322 "CTRP" @default.
- NCIT_C75508 NCIT_P366 "HIRA_wt_Allele" @default.
- NCIT_C75508 NCIT_P98 "Hemizygous deletion of chromosome 22q11.2 causes haploinsufficiency of both the HIRA gene and the TBX1 gene and is associated with the 22q11.2 deletion syndrome. The phenotype of this syndrome can include symptoms of either velocardiofacial syndrome or DiGeorge syndrome or a combination of indications for both syndromes. (OMIM)" @default.
- NCIT_C75508 NCIT_R37 NCIT_C16397 @default.
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- NCIT_C75508 NCIT_R38 NCIT_C27145 @default.
- NCIT_C75508 NCIT_R38 NCIT_C27351 @default.
- NCIT_C75508 NCIT_R38 NCIT_C27551 @default.
- NCIT_C75508 NCIT_R38 NCIT_C27872 @default.
- NCIT_C75508 NCIT_R38 NCIT_C28193 @default.
- NCIT_C75508 NCIT_R38 NCIT_C2989 @default.
- NCIT_C75508 NCIT_R38 NCIT_C2991 @default.
- NCIT_C75508 NCIT_R38 NCIT_C3101 @default.
- NCIT_C75508 NCIT_R38 NCIT_C3131 @default.
- NCIT_C75508 NCIT_R38 NCIT_C3507 @default.
- NCIT_C75508 NCIT_R38 NCIT_C7057 @default.
- NCIT_C75508 NCIT_R41 NCIT_C14182 @default.
- NCIT_C75508 NCIT_R41 NCIT_C14225 @default.
- NCIT_C75508 NCIT_R41 NCIT_C14234 @default.
- NCIT_C75508 NCIT_R41 NCIT_C14250 @default.
- NCIT_C75508 NCIT_R41 NCIT_C14262 @default.
- NCIT_C75508 NCIT_R41 NCIT_C14282 @default.
- NCIT_C75508 NCIT_R41 NCIT_C25796 @default.
- NCIT_C75508 NCIT_R41 NCIT_C79740 @default.
- NCIT_C75508 normalizedInformationContent "100" @default.
- NCIT_C75508 referenceCount "1" @default.
- NCIT_C75508 hasExactSynonym "DGCR1" @default.
- NCIT_C75508 hasExactSynonym "DiGeorge Critical Region Gene 1" @default.
- NCIT_C75508 hasExactSynonym "DiGeorge Syndrome Critical Region Gene 1" @default.
- NCIT_C75508 hasExactSynonym "HIR (Histone Cell Cycle Regulation Defective) Homolog A (S. cerevisiae) Gene" @default.
- NCIT_C75508 hasExactSynonym "HIR Histone Cell Cycle Regulation Defective Homolog A (S. cerevisiae) Gene" @default.
- NCIT_C75508 hasExactSynonym "HIR" @default.
- NCIT_C75508 hasExactSynonym "HIR, S. cerevisiae, Homolog of Gene" @default.
- NCIT_C75508 hasExactSynonym "HIRA wt Allele" @default.
- NCIT_C75508 hasExactSynonym "Histone Cell Cycle Regulation Defective, S. cerevisiae, Homolog of, A Gene" @default.
- NCIT_C75508 hasExactSynonym "Histone Cell Cycle Regulator wt Allele" @default.
- NCIT_C75508 hasExactSynonym "TUP-Like Enhancer of Split 1 Gene" @default.
- NCIT_C75508 hasExactSynonym "TUP1" @default.
- NCIT_C75508 hasExactSynonym "TUPLE1" @default.
- NCIT_C75508 inSubset NCIT_C116977 @default.
- NCIT_C75508 inSubset NCIT_C142799 @default.
- NCIT_C75508 inSubset NCIT_C142800 @default.
- NCIT_C75508 type Class @default.
- NCIT_C75508 isDefinedBy ncit.owl @default.
- NCIT_C75508 label "HIRA wt Allele" @default.
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- NCIT_C75508 subClassOf NCIT_C75507 @default.
- NCIT_C75508 subClassOf NCIT_C75508 @default.