EFHC1 protein, human

Preferred Label : EFHC1 protein, human;

MeSH note : mutations in EFHC1 cause juvenile myoclonic epilepsy; RefSeq NM_018100;

MeSH synonym : myoclonin protein, human; EF-hand domain (C-terminal) containing 1 protein, human;

Is substance : O;

Details

Origin ID

C489648;

UMLS CUI

C1506217;

MeSH indexing information
- EF hand motifs [MeSH Descriptor]
- myoclonic epilepsy, juvenile [MeSH Descriptor]
MeSH term(s) associated for indexing
- Calcium-Binding proteins [MeSH Descriptor]
Record concept(s)
- EFHC1 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)
- EF-Hand Domain-Containing Protein 1 [NCIt concept]

Keyword's position in hierarchy(ies) :

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