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- NCIT_C189069 IAO_0000115 "Human FA2H wild-type allele is located in the vicinity of 16q23.1 and is approximately 62 kb in length. This allele, which encodes fatty acid 2-hydroxylase protein, is involved in the synthesis of 2-hydroxysphingolipids, which in turn are associated with formation of plasma membrane rafts, hair follicles, the myelin sheath and epidermal lamellar bodies. Mutation of the gene is associated with leukodystrophy dysmyelinating with spastic paraparesis with or without dystonia (autosomal recessive spastic paraplegia 35)." @default.
- NCIT_C189069 NCIT_NHC0 "C189069" @default.
- NCIT_C189069 NCIT_P100 "611026" @default.
- NCIT_C189069 NCIT_P102 "BC002679" @default.
- NCIT_C189069 NCIT_P106 "Gene or Genome" @default.
- NCIT_C189069 NCIT_P108 "FA2H wt Allele" @default.
- NCIT_C189069 NCIT_P208 "CL1794258" @default.
- NCIT_C189069 NCIT_P321 "79152" @default.
- NCIT_C189069 NCIT_R130 NCIT_C18611 @default.
- NCIT_C189069 NCIT_R130 NCIT_C20633 @default.
- NCIT_C189069 NCIT_R130 NCIT_C38807 @default.
- NCIT_C189069 NCIT_R130 NCIT_C39728 @default.
- NCIT_C189069 NCIT_R37 NCIT_C157205 @default.
- NCIT_C189069 NCIT_R37 NCIT_C16944 @default.
- NCIT_C189069 NCIT_R37 NCIT_C16945 @default.
- NCIT_C189069 NCIT_R37 NCIT_C17702 @default.
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- NCIT_C189069 NCIT_R37 NCIT_C19405 @default.
- NCIT_C189069 NCIT_R37 NCIT_C19536 @default.
- NCIT_C189069 NCIT_R37 NCIT_C19899 @default.
- NCIT_C189069 NCIT_R37 NCIT_C21198 @default.
- NCIT_C189069 NCIT_R37 NCIT_C26565 @default.
- NCIT_C189069 NCIT_R37 NCIT_C28498 @default.
- NCIT_C189069 NCIT_R40 NCIT_C12219 @default.
- NCIT_C189069 NCIT_R40 NCIT_C13282 @default.
- NCIT_C189069 NCIT_R40 NCIT_C13377 @default.
- NCIT_C189069 NCIT_R40 NCIT_C13432 @default.
- NCIT_C189069 NCIT_R40 NCIT_C13446 @default.
- NCIT_C189069 NCIT_R40 NCIT_C13858 @default.
- NCIT_C189069 NCIT_R40 NCIT_C14135 @default.
- NCIT_C189069 NCIT_R40 NCIT_C32221 @default.
- NCIT_C189069 NCIT_R40 NCIT_C34070 @default.
- NCIT_C189069 NCIT_R41 NCIT_C14182 @default.
- NCIT_C189069 NCIT_R41 NCIT_C14225 @default.
- NCIT_C189069 NCIT_R41 NCIT_C14234 @default.
- NCIT_C189069 NCIT_R41 NCIT_C14250 @default.
- NCIT_C189069 NCIT_R41 NCIT_C14262 @default.
- NCIT_C189069 NCIT_R41 NCIT_C14282 @default.
- NCIT_C189069 NCIT_R41 NCIT_C25796 @default.
- NCIT_C189069 NCIT_R41 NCIT_C79740 @default.
- NCIT_C189069 normalizedInformationContent "100" @default.
- NCIT_C189069 referenceCount "1" @default.
- NCIT_C189069 hasExactSynonym "FA2H wt Allele" @default.
- NCIT_C189069 hasExactSynonym "FAAH" @default.
- NCIT_C189069 hasExactSynonym "FAH1" @default.
- NCIT_C189069 hasExactSynonym "FAH1, S. cerevisiae, Homolog of Gene" @default.
- NCIT_C189069 hasExactSynonym "FAXDC1" @default.
- NCIT_C189069 hasExactSynonym "FLJ25287" @default.
- NCIT_C189069 hasExactSynonym "Fatty Acid 2-Hydroxylase wt Allele" @default.
- NCIT_C189069 hasExactSynonym "Fatty Acid Hydroxylase Domain Containing 1 Gene" @default.
- NCIT_C189069 hasExactSynonym "Fatty Acid Hydroxylase Gene" @default.
- NCIT_C189069 hasExactSynonym "SCS7" @default.
- NCIT_C189069 hasExactSynonym "SCS7, S. cerevisiae, Homolog of Gene" @default.
- NCIT_C189069 hasExactSynonym "SPG35" @default.
- NCIT_C189069 hasExactSynonym "Spastic Paraplegia 35 (Autosomal Recessive) Gene" @default.
- NCIT_C189069 type Class @default.
- NCIT_C189069 isDefinedBy ncit.owl @default.
- NCIT_C189069 label "FA2H wt Allele" @default.
- NCIT_C189069 subClassOf NCIT_C16612 @default.
- NCIT_C189069 subClassOf NCIT_C189068 @default.
- NCIT_C189069 subClassOf NCIT_C189069 @default.
- NCIT_C189069 subClassOf NCIT_C21281 @default.
- NCIT_C189069 subClassOf NCIT_C25939 @default.
- NCIT_C189069 equivalentClass B653e3f2d6cc307ae9fcdfb7c042c8383 @default.
- NCIT_C189069 equivalentClass Bb7619436c43531296f9baca33fac85ac @default.