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- NCIT_C191661 IAO_0000115 "Human MPDU1 wild-type allele is located in the vicinity of 17p13.1 and is approximately 9 kb in length. This allele, which encodes mannose-P-dolichol utilization defect 1 protein, plays a role in the synthesis of mannose-P-dolichol, which is required for the synthesis of dolichol-linked oligosaccharides, such as glycosylphosphatidylinositols. Mutation of the gene is associated with congenital disorder of glycosylation type 1f." @default.
- NCIT_C191661 NCIT_NHC0 "C191661" @default.
- NCIT_C191661 NCIT_P100 "604041" @default.
- NCIT_C191661 NCIT_P102 "AF038961" @default.
- NCIT_C191661 NCIT_P106 "Gene or Genome" @default.
- NCIT_C191661 NCIT_P108 "MPDU1 wt Allele" @default.
- NCIT_C191661 NCIT_P208 "CL1905258" @default.
- NCIT_C191661 NCIT_P321 "9526" @default.
- NCIT_C191661 NCIT_R37 NCIT_C17019 @default.
- NCIT_C191661 NCIT_R37 NCIT_C17702 @default.
- NCIT_C191661 NCIT_R37 NCIT_C17710 @default.
- NCIT_C191661 NCIT_R37 NCIT_C17828 @default.
- NCIT_C191661 NCIT_R37 NCIT_C17933 @default.
- NCIT_C191661 NCIT_R37 NCIT_C19405 @default.
- NCIT_C191661 NCIT_R37 NCIT_C19406 @default.
- NCIT_C191661 NCIT_R37 NCIT_C19536 @default.
- NCIT_C191661 NCIT_R37 NCIT_C19899 @default.
- NCIT_C191661 NCIT_R37 NCIT_C19903 @default.
- NCIT_C191661 NCIT_R37 NCIT_C21034 @default.
- NCIT_C191661 NCIT_R37 NCIT_C21198 @default.
- NCIT_C191661 NCIT_R37 NCIT_C28498 @default.
- NCIT_C191661 NCIT_R40 NCIT_C12219 @default.
- NCIT_C191661 NCIT_R40 NCIT_C13282 @default.
- NCIT_C191661 NCIT_R40 NCIT_C13377 @default.
- NCIT_C191661 NCIT_R40 NCIT_C13432 @default.
- NCIT_C191661 NCIT_R40 NCIT_C13446 @default.
- NCIT_C191661 NCIT_R40 NCIT_C13628 @default.
- NCIT_C191661 NCIT_R40 NCIT_C14135 @default.
- NCIT_C191661 NCIT_R40 NCIT_C32221 @default.
- NCIT_C191661 NCIT_R40 NCIT_C34070 @default.
- NCIT_C191661 NCIT_R41 NCIT_C14182 @default.
- NCIT_C191661 NCIT_R41 NCIT_C14225 @default.
- NCIT_C191661 NCIT_R41 NCIT_C14234 @default.
- NCIT_C191661 NCIT_R41 NCIT_C14250 @default.
- NCIT_C191661 NCIT_R41 NCIT_C14262 @default.
- NCIT_C191661 NCIT_R41 NCIT_C14282 @default.
- NCIT_C191661 NCIT_R41 NCIT_C25796 @default.
- NCIT_C191661 NCIT_R41 NCIT_C79740 @default.
- NCIT_C191661 normalizedInformationContent "100" @default.
- NCIT_C191661 referenceCount "1" @default.
- NCIT_C191661 hasExactSynonym "CDGIF" @default.
- NCIT_C191661 hasExactSynonym "CDGIf" @default.
- NCIT_C191661 hasExactSynonym "HBEBP2BPA" @default.
- NCIT_C191661 hasExactSynonym "LEC35" @default.
- NCIT_C191661 hasExactSynonym "Lec35" @default.
- NCIT_C191661 hasExactSynonym "MPDU1 wt Allele" @default.
- NCIT_C191661 hasExactSynonym "Mannose-P-Dolichol Utilization Defect 1 wt Allele" @default.
- NCIT_C191661 hasExactSynonym "My008" @default.
- NCIT_C191661 hasExactSynonym "PP3958" @default.
- NCIT_C191661 hasExactSynonym "PQLC5" @default.
- NCIT_C191661 hasExactSynonym "SL15" @default.
- NCIT_C191661 hasExactSynonym "SLC66A5" @default.
- NCIT_C191661 hasExactSynonym "Suppressor of Lec15 Gene" @default.
- NCIT_C191661 hasExactSynonym "Suppressor of Lec15 and Lec35 Glycosylation Mutation Homolog Gene" @default.
- NCIT_C191661 type Class @default.
- NCIT_C191661 isDefinedBy ncit.owl @default.
- NCIT_C191661 label "MPDU1 wt Allele" @default.
- NCIT_C191661 subClassOf B0e08039761c8aca89056b0aafe2c322b @default.
- NCIT_C191661 subClassOf B2e39b5cea4e9e8e691093092917275eb @default.
- NCIT_C191661 subClassOf NCIT_C16612 @default.
- NCIT_C191661 subClassOf NCIT_C191660 @default.
- NCIT_C191661 subClassOf NCIT_C191661 @default.
- NCIT_C191661 subClassOf NCIT_C20194 @default.