GLI3 protein, human

Preferred Label : GLI3 protein, human;

MeSH note : defects in GLI3 are a cause of: Pallister-Hall syndrome (PHS), type a1/b postaxial polydactyly (PAPA1/PAPB), and type IV preaxial polydactyly; RefSeq NM_000168;

MeSH synonym : GLI-Kruppel family member GLI3 (Greig cephalopolysyndactyly syndrome) protein, human; GLI family zinc finger 3 protein, human;

Is substance : O;

Details

Origin ID

C065683;

UMLS CUI

C0082708;

MeSH term(s) associated for indexing
- Kruppel-Like transcription factors [MeSH Descriptor]
- Zinc Finger Protein Gli3 [MeSH Descriptor]
- nerve tissue proteins [MeSH Descriptor]
Record concept(s)
- GLI3 protein, human [MeSH concept]
Semantic type(s)
- Amino Acid, Peptide, or Protein [UMLS semantic type]
- Biologically Active Substance [UMLS semantic type]
UMLS correspondences (same concept)
- Zinc Finger Protein GLI3 [NCIt concept]

Keyword's position in hierarchy(ies) :

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