KCTD7 protein, human

Preferred Label : KCTD7 protein, human;

MeSH note : mutation in gene is linked to progressive myoclonic epilepsy; RefSeq NM_153033.1; NP_694578.1;

MeSH synonym : potassium channel tetramerisation domain containing 7 protein, human;

Is substance : O;

Details

Origin ID

C522280;

UMLS CUI

C2001347;

MeSH term(s) associated for indexing
- potassium channels [MeSH Descriptor]
Record concept(s)
- KCTD7 protein, human [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) :

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