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- NCIT_C179876 IAO_0000115 "Human ANO6 wild-type allele is located in the vicinity of 12q12 and is approximately 266 kb in length. This allele, which encodes anoctamin-6 protein, is involved in phospholipid scrambling. A splice acceptor site mutation is associated with Scott syndrome." @default.
- NCIT_C179876 NCIT_NHC0 "C179876" @default.
- NCIT_C179876 NCIT_P100 "608663" @default.
- NCIT_C179876 NCIT_P102 "AL832340" @default.
- NCIT_C179876 NCIT_P106 "Gene or Genome" @default.
- NCIT_C179876 NCIT_P108 "ANO6 wt Allele" @default.
- NCIT_C179876 NCIT_P208 "CL1662366" @default.
- NCIT_C179876 NCIT_P321 "196527" @default.
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- NCIT_C179876 normalizedInformationContent "100" @default.
- NCIT_C179876 referenceCount "1" @default.
- NCIT_C179876 hasExactSynonym "ANO6 wt Allele" @default.
- NCIT_C179876 hasExactSynonym "Anoctamin 6 wt Allele" @default.
- NCIT_C179876 hasExactSynonym "BDPLT7" @default.
- NCIT_C179876 hasExactSynonym "DKFZp313M0720" @default.
- NCIT_C179876 hasExactSynonym "SCTS" @default.
- NCIT_C179876 hasExactSynonym "TMEM16F" @default.
- NCIT_C179876 type Class @default.
- NCIT_C179876 isDefinedBy ncit.owl @default.
- NCIT_C179876 label "ANO6 wt Allele" @default.
- NCIT_C179876 subClassOf B69d0a9d1ac036312ac10afed7ef84a7b @default.
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- NCIT_C179876 subClassOf NCIT_C25993 @default.
- NCIT_C179876 subClassOf NCIT_C26039 @default.
- NCIT_C179876 subClassOf NCIT_C28533 @default.