FKBP14 protein, human

Preferred Label : FKBP14 protein, human;

MeSH note : mutations in FKBP14 cause a variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss;

Registry Number MeSH : EC 5.2.1.8;

Is substance : O;

UNII : EC 5.2.1.8;

Détails

Origin ID

C572897;

UMLS CUI

C3492840;

Automatic exact mappings (from CISMeF team)
- Serine/Threonine-Protein Phosphatase 2A Activator [NCIt concept]
MeSH indexing information
- ehlers-danlos syndrome [MeSH Descriptor]
MeSH term(s) associated for indexing
- peptidylprolyl isomerase [MeSH Descriptor]
Record concept(s)
- FKBP14 protein, human [MeSH concept]
Semantic type(s)
- Amino Acid, Peptide, or Protein [UMLS semantic type]

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