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- NCIT_C191879 IAO_0000115 "Human ABCD4 wild-type allele is located in the vicinity of 14q24.3 and is approximately 18 kb in length. This allele, which encodes lysosomal cobalamin transporter ABCD4 protein, is involved in the cellular localization of vitamin B12. Mutation of the gene is associated with methylmalonic aciduria and homocystinuria, cblJ type." @default.
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- NCIT_C191879 NCIT_P106 "Gene or Genome" @default.
- NCIT_C191879 NCIT_P108 "ABCD4 wt Allele" @default.
- NCIT_C191879 NCIT_P208 "CL1905125" @default.
- NCIT_C191879 NCIT_P321 "5826" @default.
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- NCIT_C191879 NCIT_R40 NCIT_C34070 @default.
- NCIT_C191879 NCIT_R41 NCIT_C14182 @default.
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- NCIT_C191879 NCIT_R41 NCIT_C25796 @default.
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- NCIT_C191879 normalizedInformationContent "100" @default.
- NCIT_C191879 referenceCount "1" @default.
- NCIT_C191879 hasExactSynonym "ABC41" @default.
- NCIT_C191879 hasExactSynonym "ABCD4 wt Allele" @default.
- NCIT_C191879 hasExactSynonym "ATP Binding Cassette Subfamily D Member 4 wt Allele" @default.
- NCIT_C191879 hasExactSynonym "ATP-Binding Cassette, Sub-Family D (ALD), Member 4 Gene" @default.
- NCIT_C191879 hasExactSynonym "ATP-Binding Cassette, Subfamily D, Member 4 Gene" @default.
- NCIT_C191879 hasExactSynonym "EST352188" @default.
- NCIT_C191879 hasExactSynonym "MAHCJ" @default.
- NCIT_C191879 hasExactSynonym "P70R" @default.
- NCIT_C191879 hasExactSynonym "P79R" @default.
- NCIT_C191879 hasExactSynonym "PMP69" @default.
- NCIT_C191879 hasExactSynonym "PXMP1L" @default.
- NCIT_C191879 type Class @default.
- NCIT_C191879 isDefinedBy ncit.owl @default.
- NCIT_C191879 label "ABCD4 wt Allele" @default.
- NCIT_C191879 subClassOf NCIT_C158414 @default.
- NCIT_C191879 subClassOf NCIT_C16612 @default.
- NCIT_C191879 subClassOf NCIT_C191877 @default.
- NCIT_C191879 subClassOf NCIT_C191879 @default.
- NCIT_C191879 subClassOf NCIT_C21281 @default.
- NCIT_C191879 subClassOf NCIT_C21295 @default.
- NCIT_C191879 subClassOf NCIT_C28533 @default.
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