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- NCIT_C151925 IAO_0000115 "Human ANKRD26 wild-type allele is located in the vicinity of 10p12.1 and is approximately 134 kb in length. This allele, which encodes ankyrin repeat domain-containing protein 26, is involved in adipogenesis, appetite and platelet functions. Mutations in the 5' promoter region of this gene that result in increased expression are associated with autosomal dominant thrombocytopenia 2." @default.
- NCIT_C151925 NCIT_NHC0 "C151925" @default.
- NCIT_C151925 NCIT_P100 "610855" @default.
- NCIT_C151925 NCIT_P102 "AB028997" @default.
- NCIT_C151925 NCIT_P106 "Gene or Genome" @default.
- NCIT_C151925 NCIT_P107 "ANKRD26 wt Allele" @default.
- NCIT_C151925 NCIT_P108 "ANKRD26 wt Allele" @default.
- NCIT_C151925 NCIT_P208 "CL553264" @default.
- NCIT_C151925 NCIT_P321 "22852" @default.
- NCIT_C151925 NCIT_P322 "CTRP" @default.
- NCIT_C151925 NCIT_P98 "Pseudogenes of the ANKRD26 gene are found on chromosome 7, 10, 13 and 16." @default.
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- NCIT_C151925 normalizedInformationContent "100" @default.
- NCIT_C151925 referenceCount "1" @default.
- NCIT_C151925 hasExactSynonym "ANKRD26 wt Allele" @default.
- NCIT_C151925 hasExactSynonym "Ankyrin Repeat Domain 26 wt Allele" @default.
- NCIT_C151925 hasExactSynonym "KIAA1074" @default.
- NCIT_C151925 hasExactSynonym "THC2" @default.
- NCIT_C151925 hasExactSynonym "Thrombocytopenia 2 (Autosomal Dominant) Gene" @default.
- NCIT_C151925 hasExactSynonym "bA145E8.1" @default.
- NCIT_C151925 inSubset NCIT_C116977 @default.
- NCIT_C151925 inSubset NCIT_C142799 @default.
- NCIT_C151925 inSubset NCIT_C142800 @default.
- NCIT_C151925 type Class @default.
- NCIT_C151925 isDefinedBy ncit.owl @default.
- NCIT_C151925 label "ANKRD26 wt Allele" @default.
- NCIT_C151925 subClassOf Be564f711d7875c9e93c724904a5bbca9 @default.
- NCIT_C151925 subClassOf Be67b817a6e2a37f9c5752095913fa40e @default.
- NCIT_C151925 subClassOf NCIT_C151924 @default.
- NCIT_C151925 subClassOf NCIT_C151925 @default.
- NCIT_C151925 subClassOf NCIT_C16612 @default.
- NCIT_C151925 subClassOf NCIT_C20194 @default.