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- NCIT_C177663 IAO_0000115 "Human KIF1C wild-type allele is located in the vicinity of 17p13.2 and is approximately 30 kb in length. This allele, which encodes kinesin-like protein KIF1C, is involved in Golgi to ER transport along microtubules. Mutations in the gene are associated with autosomal recessive spastic ataxia 2." @default.
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- NCIT_C177663 NCIT_P106 "Gene or Genome" @default.
- NCIT_C177663 NCIT_P108 "KIF1C wt Allele" @default.
- NCIT_C177663 NCIT_P208 "CL1643481" @default.
- NCIT_C177663 NCIT_P321 "10749" @default.
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- NCIT_C177663 normalizedInformationContent "100" @default.
- NCIT_C177663 referenceCount "1" @default.
- NCIT_C177663 hasExactSynonym "KIAA0706" @default.
- NCIT_C177663 hasExactSynonym "KIF1C wt Allele" @default.
- NCIT_C177663 hasExactSynonym "Kinesin Family Member 1C wt Allele" @default.
- NCIT_C177663 hasExactSynonym "LTXS1" @default.
- NCIT_C177663 hasExactSynonym "LTXS1, Mouse, Homolog of Gene" @default.
- NCIT_C177663 hasExactSynonym "SATX2" @default.
- NCIT_C177663 hasExactSynonym "SAX2" @default.
- NCIT_C177663 hasExactSynonym "SPAX2" @default.
- NCIT_C177663 hasExactSynonym "SPG58" @default.
- NCIT_C177663 hasExactSynonym "Spastic Ataxia 2 (Autosomal Recessive) Gene" @default.
- NCIT_C177663 type Class @default.
- NCIT_C177663 isDefinedBy ncit.owl @default.
- NCIT_C177663 label "KIF1C wt Allele" @default.
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