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- NCIT_C190257 IAO_0000115 "Human KRT12 wild-type allele is located in the vicinity of 17q21.2 and is approximately 6 kb in length. This allele, which encodes keratin, type I cytoskeletal 12 protein, is involved in the structure of intermediate filaments in the anterior corneal epithelium. Mutation of the gene is associated with Meesmann corneal dystrophy 1." @default.
- NCIT_C190257 NCIT_NHC0 "C190257" @default.
- NCIT_C190257 NCIT_P100 "601687" @default.
- NCIT_C190257 NCIT_P102 "NM_000223" @default.
- NCIT_C190257 NCIT_P106 "Gene or Genome" @default.
- NCIT_C190257 NCIT_P108 "KRT12 wt Allele" @default.
- NCIT_C190257 NCIT_P208 "CL1799046" @default.
- NCIT_C190257 NCIT_P321 "3859" @default.
- NCIT_C190257 NCIT_R37 NCIT_C161550 @default.
- NCIT_C190257 NCIT_R37 NCIT_C17729 @default.
- NCIT_C190257 NCIT_R37 NCIT_C17828 @default.
- NCIT_C190257 NCIT_R37 NCIT_C19413 @default.
- NCIT_C190257 NCIT_R37 NCIT_C20480 @default.
- NCIT_C190257 NCIT_R37 NCIT_C20748 @default.
- NCIT_C190257 NCIT_R37 NCIT_C20768 @default.
- NCIT_C190257 NCIT_R37 NCIT_C21124 @default.
- NCIT_C190257 NCIT_R37 NCIT_C21128 @default.
- NCIT_C190257 NCIT_R37 NCIT_C21147 @default.
- NCIT_C190257 NCIT_R37 NCIT_C40795 @default.
- NCIT_C190257 NCIT_R37 NCIT_C41517 @default.
- NCIT_C190257 NCIT_R40 NCIT_C12219 @default.
- NCIT_C190257 NCIT_R40 NCIT_C13282 @default.
- NCIT_C190257 NCIT_R40 NCIT_C13377 @default.
- NCIT_C190257 NCIT_R40 NCIT_C13432 @default.
- NCIT_C190257 NCIT_R40 NCIT_C13446 @default.
- NCIT_C190257 NCIT_R40 NCIT_C14135 @default.
- NCIT_C190257 NCIT_R40 NCIT_C25987 @default.
- NCIT_C190257 NCIT_R40 NCIT_C32221 @default.
- NCIT_C190257 NCIT_R40 NCIT_C34070 @default.
- NCIT_C190257 NCIT_R41 NCIT_C14182 @default.
- NCIT_C190257 NCIT_R41 NCIT_C14225 @default.
- NCIT_C190257 NCIT_R41 NCIT_C14234 @default.
- NCIT_C190257 NCIT_R41 NCIT_C14250 @default.
- NCIT_C190257 NCIT_R41 NCIT_C14262 @default.
- NCIT_C190257 NCIT_R41 NCIT_C14282 @default.
- NCIT_C190257 NCIT_R41 NCIT_C25796 @default.
- NCIT_C190257 NCIT_R41 NCIT_C79740 @default.
- NCIT_C190257 normalizedInformationContent "100" @default.
- NCIT_C190257 referenceCount "1" @default.
- NCIT_C190257 hasExactSynonym "CK-12" @default.
- NCIT_C190257 hasExactSynonym "Cytokeratin 12 Gene" @default.
- NCIT_C190257 hasExactSynonym "K12" @default.
- NCIT_C190257 hasExactSynonym "KA12" @default.
- NCIT_C190257 hasExactSynonym "KRT12 wt Allele" @default.
- NCIT_C190257 hasExactSynonym "Keratin 12 wt Allele" @default.
- NCIT_C190257 hasExactSynonym "Keratin 12, Type I Gene" @default.
- NCIT_C190257 hasExactSynonym "Keratin, Type I Cytoskeletal 12 Gene" @default.
- NCIT_C190257 hasExactSynonym "MECD1" @default.
- NCIT_C190257 hasExactSynonym "Meesmann Corneal Dystrophy Gene" @default.
- NCIT_C190257 type Class @default.
- NCIT_C190257 isDefinedBy ncit.owl @default.
- NCIT_C190257 label "KRT12 wt Allele" @default.
- NCIT_C190257 subClassOf B598af66ead1b90489b54eab7f024591b @default.
- NCIT_C190257 subClassOf B72fd0923a8e8b5278f0ad5dfb49e7fc3 @default.
- NCIT_C190257 subClassOf NCIT_C16612 @default.
- NCIT_C190257 subClassOf NCIT_C190256 @default.
- NCIT_C190257 subClassOf NCIT_C190257 @default.
- NCIT_C190257 subClassOf NCIT_C20744 @default.
- NCIT_C190257 subClassOf NCIT_C20745 @default.
- NCIT_C190257 subClassOf NCIT_C30073 @default.