" /> GLI3 wt Allele - CISMeF





Preferred Label : GLI3 wt Allele;

NCIt synonyms : GLI-Kruppel Family Member 3; PHS; PAP-A; GCPS; GLI-Kruppel Family Member GLI3 (Greig Cephalopolysyndactyly Syndrome) wt Allele; PAPA; ACLS; PAPA1; PPDIV; GLI3FL; GCPS-190; PAPB;

NCIt definition : Human GLI3 wild-type allele is located in the vicinity of 7p13 and is approximately 272 kb in length. This allele, which encodes zinc finger protein GLI3, plays a role in the regulation of sonic hedgehog-dependent transcription of specific genes during the development of multiple organ systems. This gene is the site of a mutation that is linked to Greig cephalopolysyndactyly syndrome.;

NCIt note : The GLI3 gene product plays a role in development of the central nervous system, the esophagus, trachea, lung and limbs (Genatlas).;

GenBank Accession Number : NM_000168;

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10/05/2025


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