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- NCIT_C75523 IAO_0000115 "Human TRPS1 wild-type allele is located in the vicinity of 8q24.12 and is approximately 261 kb in length. This allele, which encodes zinc finger transcription factor Trps1 protein, plays a role in regulation of bone and hair development. Mutations in this gene are associated with Type 1 trichorhinophalangeal syndrome." @default.
- NCIT_C75523 NCIT_NHC0 "C75523" @default.
- NCIT_C75523 NCIT_P100 "604386" @default.
- NCIT_C75523 NCIT_P102 "NM_014112" @default.
- NCIT_C75523 NCIT_P106 "Gene or Genome" @default.
- NCIT_C75523 NCIT_P108 "TRPS1 wt Allele" @default.
- NCIT_C75523 NCIT_P207 "C2699875" @default.
- NCIT_C75523 NCIT_P321 "7227" @default.
- NCIT_C75523 NCIT_P366 "TRPS1_wt_Allele" @default.
- NCIT_C75523 NCIT_P98 "The trichorhinophalangeal syndrome type II, or Langer-Giedion syndrome, is a contiguous gene syndrome due to loss of functional copies of both the TRPS1 and EXT1 genes. (Hum Mol Genet. 1995; 4: 31-6.)" @default.
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- NCIT_C75523 hasExactSynonym "GC79" @default.
- NCIT_C75523 hasExactSynonym "MGC134928" @default.
- NCIT_C75523 hasExactSynonym "TRPS1 wt Allele" @default.
- NCIT_C75523 hasExactSynonym "Trichorhinophalangeal Syndrome I wt Allele" @default.
- NCIT_C75523 type Class @default.
- NCIT_C75523 isDefinedBy ncit.owl @default.
- NCIT_C75523 label "TRPS1 wt Allele" @default.
- NCIT_C75523 subClassOf NCIT_C16612 @default.
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