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- NCIT_C177179 IAO_0000115 "Human SLC24A5 wild-type allele is located in the vicinity of 15q21.1 and is approximately 22 kb in length. This allele, which encodes sodium/potassium/calcium exchanger 5 protein, is involved in melanosome pigmentation. Mutation of the gene is associated with oculocutaneous albinism type 6." @default.
- NCIT_C177179 NCIT_NHC0 "C177179" @default.
- NCIT_C177179 NCIT_P100 "609802" @default.
- NCIT_C177179 NCIT_P102 "AF348468" @default.
- NCIT_C177179 NCIT_P106 "Gene or Genome" @default.
- NCIT_C177179 NCIT_P108 "SLC24A5 wt Allele" @default.
- NCIT_C177179 NCIT_P208 "CL1643108" @default.
- NCIT_C177179 NCIT_P321 "283652" @default.
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- NCIT_C177179 NCIT_R41 NCIT_C79740 @default.
- NCIT_C177179 normalizedInformationContent "100" @default.
- NCIT_C177179 referenceCount "1" @default.
- NCIT_C177179 hasExactSynonym "JSX" @default.
- NCIT_C177179 hasExactSynonym "NCKX5" @default.
- NCIT_C177179 hasExactSynonym "OCA6" @default.
- NCIT_C177179 hasExactSynonym "Oculocutaneous Albinism 6 (Autosomal Recessive) Gene" @default.
- NCIT_C177179 hasExactSynonym "SHEP4" @default.
- NCIT_C177179 hasExactSynonym "SLC24A5 wt Allele" @default.
- NCIT_C177179 hasExactSynonym "Solute Carrier Family 24 (Sodium/Potassium/Calcium Exchanger), Member 5 Gene" @default.
- NCIT_C177179 hasExactSynonym "Solute Carrier Family 24 Member 5 wt Allele" @default.
- NCIT_C177179 hasExactSynonym "Solute Carrier Family 24, Member 5 Gene" @default.
- NCIT_C177179 type Class @default.
- NCIT_C177179 isDefinedBy ncit.owl @default.
- NCIT_C177179 label "SLC24A5 wt Allele" @default.
- NCIT_C177179 subClassOf B91def93389412e9b4f6924437aaff95b @default.
- NCIT_C177179 subClassOf Bad235c768f4254189159d3a5e021e87e @default.
- NCIT_C177179 subClassOf NCIT_C16612 @default.
- NCIT_C177179 subClassOf NCIT_C177178 @default.
- NCIT_C177179 subClassOf NCIT_C177179 @default.
- NCIT_C177179 subClassOf NCIT_C21295 @default.
- NCIT_C177179 subClassOf NCIT_C28533 @default.