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- NCIT_C102952 IAO_0000115 "Human OTX2 wild-type allele is located in the vicinity of 14q22.3 and is approximately 10 kb in length. This allele, which encodes homeobox protein OTX2, plays a role in the positive regulation of gene expression during embryonic pattern formation. Mutation of the gene is associated with both microphthalmia syndromic type 5 and pituitary hormone deficiency combined type 6." @default.
- NCIT_C102952 NCIT_NHC0 "C102952" @default.
- NCIT_C102952 NCIT_P100 "600037" @default.
- NCIT_C102952 NCIT_P102 "AF298117" @default.
- NCIT_C102952 NCIT_P106 "Gene or Genome" @default.
- NCIT_C102952 NCIT_P107 "OTX2 wt Allele" @default.
- NCIT_C102952 NCIT_P108 "OTX2 wt Allele" @default.
- NCIT_C102952 NCIT_P207 "C3539601" @default.
- NCIT_C102952 NCIT_P321 "5015" @default.
- NCIT_C102952 NCIT_P322 "CTRP" @default.
- NCIT_C102952 NCIT_P98 "Aberrant expression of the OTX2 gene may be associated with subgroup 3 medulloblastoma. (Nature. 2012; 488:49-56.)" @default.
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- NCIT_C102952 NCIT_R37 NCIT_C16649 @default.
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- NCIT_C102952 NCIT_R37 NCIT_C19970 @default.
- NCIT_C102952 NCIT_R37 NCIT_C19986 @default.
- NCIT_C102952 NCIT_R37 NCIT_C19988 @default.
- NCIT_C102952 NCIT_R37 NCIT_C20480 @default.
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- NCIT_C102952 NCIT_R37 NCIT_C21124 @default.
- NCIT_C102952 NCIT_R37 NCIT_C21147 @default.
- NCIT_C102952 NCIT_R37 NCIT_C28498 @default.
- NCIT_C102952 NCIT_R37 NCIT_C40523 @default.
- NCIT_C102952 NCIT_R41 NCIT_C14182 @default.
- NCIT_C102952 NCIT_R41 NCIT_C14225 @default.
- NCIT_C102952 NCIT_R41 NCIT_C14234 @default.
- NCIT_C102952 NCIT_R41 NCIT_C14250 @default.
- NCIT_C102952 NCIT_R41 NCIT_C14262 @default.
- NCIT_C102952 NCIT_R41 NCIT_C14282 @default.
- NCIT_C102952 NCIT_R41 NCIT_C25796 @default.
- NCIT_C102952 NCIT_R41 NCIT_C79740 @default.
- NCIT_C102952 normalizedInformationContent "100" @default.
- NCIT_C102952 referenceCount "1" @default.
- NCIT_C102952 hasExactSynonym "CPHD6" @default.
- NCIT_C102952 hasExactSynonym "MCOPS5" @default.
- NCIT_C102952 hasExactSynonym "OTX2 wt Allele" @default.
- NCIT_C102952 hasExactSynonym "Orthodenticle Homeobox 2 wt Allele" @default.
- NCIT_C102952 inSubset NCIT_C116977 @default.
- NCIT_C102952 inSubset NCIT_C142799 @default.
- NCIT_C102952 inSubset NCIT_C142800 @default.
- NCIT_C102952 type Class @default.
- NCIT_C102952 isDefinedBy ncit.owl @default.
- NCIT_C102952 label "OTX2 wt Allele" @default.
- NCIT_C102952 subClassOf NCIT_C102951 @default.
- NCIT_C102952 subClassOf NCIT_C102952 @default.
- NCIT_C102952 subClassOf NCIT_C16612 @default.
- NCIT_C102952 subClassOf NCIT_C16615 @default.
- NCIT_C102952 subClassOf NCIT_C20420 @default.
- NCIT_C102952 subClassOf NCIT_C54362 @default.