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- NCIT_C99627 IAO_0000115 "Human TCTN1 wild-type allele is located in the vicinity of 12q24.11 and is approximately 35 kb in length. This allele, which encodes tectonic-1 protein, is involved in the modulation of hedgehog signal transduction. A mutation in the gene is associated with Joubert syndrome." @default.
- NCIT_C99627 NCIT_NHC0 "C99627" @default.
- NCIT_C99627 NCIT_P100 "609863" @default.
- NCIT_C99627 NCIT_P102 "AK055891" @default.
- NCIT_C99627 NCIT_P106 "Gene or Genome" @default.
- NCIT_C99627 NCIT_P108 "TCTN1 wt Allele" @default.
- NCIT_C99627 NCIT_P207 "C3274834" @default.
- NCIT_C99627 NCIT_P321 "79600" @default.
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- NCIT_C99627 NCIT_R41 NCIT_C25796 @default.
- NCIT_C99627 NCIT_R41 NCIT_C79740 @default.
- NCIT_C99627 normalizedInformationContent "100" @default.
- NCIT_C99627 referenceCount "1" @default.
- NCIT_C99627 hasExactSynonym "FLJ21127" @default.
- NCIT_C99627 hasExactSynonym "JBTS13" @default.
- NCIT_C99627 hasExactSynonym "TCTN1 wt Allele" @default.
- NCIT_C99627 hasExactSynonym "TECT1" @default.
- NCIT_C99627 hasExactSynonym "Tectonic 1 Gene" @default.
- NCIT_C99627 hasExactSynonym "Tectonic Family Member 1 wt Allele" @default.
- NCIT_C99627 hasExactSynonym "Tectonic Family, Member 1 Gene" @default.
- NCIT_C99627 hasExactSynonym "Tectonic Gene" @default.
- NCIT_C99627 hasExactSynonym "UNQ9369/PRO34160" @default.
- NCIT_C99627 type Class @default.
- NCIT_C99627 isDefinedBy ncit.owl @default.
- NCIT_C99627 label "TCTN1 wt Allele" @default.
- NCIT_C99627 subClassOf B022beda92be250d857f14907bd4e0697 @default.
- NCIT_C99627 subClassOf B1f71bae0bf90e3d4e80ec618e90b400f @default.
- NCIT_C99627 subClassOf NCIT_C16612 @default.
- NCIT_C99627 subClassOf NCIT_C20921 @default.
- NCIT_C99627 subClassOf NCIT_C99626 @default.
- NCIT_C99627 subClassOf NCIT_C99627 @default.