MSX2 protein - CISMeF

Preferred Label : MSX2 protein;

MeSH note : mutation in the homeodomain of the human MSX2 gene occurs in a family affected with autosomal dominant craniosynostosis, Boston type; aa sequence given in first source;

CISMeF synonym : MSX2 protein, human; Msx2 protein, mouse; Msx2 protein, rat;

MeSH synonym : MSX-2 protein;

MeSH hyponym : homeo box, msh-like 2 protein, mouse; msh homeo box homolog 2 (Drosophila) protein, rat; msh homeo box homolog 2 (Drosophila), human;

Is substance : O;

Details

Origin ID

C084119;

UMLS CUI

C0248606;

MeSH indexing information
- homeodomain proteins [MeSH Descriptor]
MeSH term(s) associated for indexing
- homeodomain proteins [MeSH Descriptor]
Record concept(s)
- MSX2 protein [MeSH concept]
- MSX2 protein, human [MeSH concept]
- Msx2 protein, mouse [MeSH concept]
- Msx2 protein, rat [MeSH concept]
Semantic type(s)
- Amino Acid, Peptide, or Protein [UMLS semantic type]
- Biologically Active Substance [UMLS semantic type]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients