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- NCIT_C91786 IAO_0000115 "Human RUNX2 wild-type allele is located in the vicinity of 6p21 and is approximately 223 kb in length. This allele, which encodes runt-related transcription factor 2 protein, is involved in osteoblastic differentiation, skeletal morphogenesis and hematopoietic stem cell differentiation. Mutation of the gene is associated with cleidocranial dysplasia." @default.
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- NCIT_C91786 NCIT_P107 "RUNX2 wt Allele" @default.
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- NCIT_C91786 hasExactSynonym "AML3" @default.
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- NCIT_C91786 hasExactSynonym "RUNX2 wt Allele" @default.
- NCIT_C91786 hasExactSynonym "Runt-Related Transcription Factor 2 wt Allele" @default.
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