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- NCIT_C75731 IAO_0000115 "Human MID1 wild-type allele is located in the vicinity of Xp22.2 and is approximately 388 kb in length. This allele, which encodes E3 ubiquitin-protein ligase Midline-1 protein, plays a role in the modulation of microtubule organization. Mutations in this gene may be associated with the X-linked form of Opitz syndrome." @default.
- NCIT_C75731 NCIT_NHC0 "C75731" @default.
- NCIT_C75731 NCIT_P100 "300552" @default.
- NCIT_C75731 NCIT_P102 "Y13667" @default.
- NCIT_C75731 NCIT_P106 "Gene or Genome" @default.
- NCIT_C75731 NCIT_P108 "MID1 wt Allele" @default.
- NCIT_C75731 NCIT_P207 "C2697964" @default.
- NCIT_C75731 NCIT_P321 "4281" @default.
- NCIT_C75731 NCIT_P366 "MID1_wt_Allele" @default.
- NCIT_C75731 NCIT_R130 NCIT_C18611 @default.
- NCIT_C75731 NCIT_R130 NCIT_C20633 @default.
- NCIT_C75731 NCIT_R130 NCIT_C38881 @default.
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- NCIT_C75731 NCIT_R37 NCIT_C17019 @default.
- NCIT_C75731 NCIT_R37 NCIT_C17710 @default.
- NCIT_C75731 NCIT_R37 NCIT_C17828 @default.
- NCIT_C75731 NCIT_R37 NCIT_C18104 @default.
- NCIT_C75731 NCIT_R37 NCIT_C19358 @default.
- NCIT_C75731 NCIT_R37 NCIT_C19406 @default.
- NCIT_C75731 NCIT_R37 NCIT_C19536 @default.
- NCIT_C75731 NCIT_R37 NCIT_C19903 @default.
- NCIT_C75731 NCIT_R37 NCIT_C19986 @default.
- NCIT_C75731 NCIT_R37 NCIT_C20480 @default.
- NCIT_C75731 NCIT_R37 NCIT_C21198 @default.
- NCIT_C75731 NCIT_R37 NCIT_C21243 @default.
- NCIT_C75731 NCIT_R37 NCIT_C21588 @default.
- NCIT_C75731 NCIT_R37 NCIT_C28498 @default.
- NCIT_C75731 NCIT_R37 NCIT_C40795 @default.
- NCIT_C75731 NCIT_R37 NCIT_C40798 @default.
- NCIT_C75731 NCIT_R37 NCIT_C61559 @default.
- NCIT_C75731 NCIT_R40 NCIT_C12219 @default.
- NCIT_C75731 NCIT_R40 NCIT_C13282 @default.
- NCIT_C75731 NCIT_R40 NCIT_C13377 @default.
- NCIT_C75731 NCIT_R40 NCIT_C13432 @default.
- NCIT_C75731 NCIT_R40 NCIT_C13446 @default.
- NCIT_C75731 NCIT_R40 NCIT_C14017 @default.
- NCIT_C75731 NCIT_R40 NCIT_C14135 @default.
- NCIT_C75731 NCIT_R40 NCIT_C32221 @default.
- NCIT_C75731 NCIT_R40 NCIT_C34070 @default.
- NCIT_C75731 NCIT_R41 NCIT_C14182 @default.
- NCIT_C75731 NCIT_R41 NCIT_C14225 @default.
- NCIT_C75731 NCIT_R41 NCIT_C14234 @default.
- NCIT_C75731 NCIT_R41 NCIT_C14250 @default.
- NCIT_C75731 NCIT_R41 NCIT_C14262 @default.
- NCIT_C75731 NCIT_R41 NCIT_C14282 @default.
- NCIT_C75731 NCIT_R41 NCIT_C25796 @default.
- NCIT_C75731 NCIT_R41 NCIT_C79740 @default.
- NCIT_C75731 normalizedInformationContent "100" @default.
- NCIT_C75731 referenceCount "1" @default.
- NCIT_C75731 hasExactSynonym "BBBG1" @default.
- NCIT_C75731 hasExactSynonym "FXY" @default.
- NCIT_C75731 hasExactSynonym "Finger on X and Y, Mouse, Homolog of Gene" @default.
- NCIT_C75731 hasExactSynonym "GBBB1" @default.
- NCIT_C75731 hasExactSynonym "MID1 wt Allele" @default.
- NCIT_C75731 hasExactSynonym "MIDIN" @default.
- NCIT_C75731 hasExactSynonym "Midline 1 (Opitz/BBB Syndrome) Gene" @default.
- NCIT_C75731 hasExactSynonym "Midline 1 RING Finger Gene" @default.
- NCIT_C75731 hasExactSynonym "Midline 1 wt Allele" @default.
- NCIT_C75731 hasExactSynonym "OGS1" @default.
- NCIT_C75731 hasExactSynonym "OS" @default.
- NCIT_C75731 hasExactSynonym "OSX" @default.
- NCIT_C75731 hasExactSynonym "RNF59" @default.
- NCIT_C75731 hasExactSynonym "TRIM18" @default.
- NCIT_C75731 hasExactSynonym "XPRF" @default.
- NCIT_C75731 hasExactSynonym "ZNFXY" @default.
- NCIT_C75731 hasExactSynonym "Zinc Finger on X and Y, Mouse, Homolog of Gene" @default.
- NCIT_C75731 type Class @default.
- NCIT_C75731 isDefinedBy ncit.owl @default.
- NCIT_C75731 label "MID1 wt Allele" @default.
- NCIT_C75731 subClassOf NCIT_C133710 @default.
- NCIT_C75731 subClassOf NCIT_C16612 @default.
- NCIT_C75731 subClassOf NCIT_C21281 @default.
- NCIT_C75731 subClassOf NCIT_C25870 @default.
- NCIT_C75731 subClassOf NCIT_C75730 @default.
- NCIT_C75731 subClassOf NCIT_C75731 @default.
- NCIT_C75731 equivalentClass B17ef2727a9155057495127341a85bc06 @default.
- NCIT_C75731 equivalentClass B4f510cb1669e72c8e834b786776a63f4 @default.