CPLANE1 protein, human

Preferred Label : CPLANE1 protein, human;

MeSH note : mutations of this protein lead to Joubert syndrome; RefSeq NM_023073;

MeSH synonym : JBTS17 protein, human; chromosome 5 open reading frame 42 protein, human; FLJ13231 protein, human; C5orf42 protein, human; ciliogenesis and planar polarity effector 1 protein, human;

Is substance : O;

Details

Origin ID

C572460;

UMLS CUI

C3492470;

MeSH term(s) associated for indexing
- membrane proteins [MeSH Descriptor]
Record concept(s)
- CPLANE1 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)
- Ciliogenesis and Planar Polarity Effector 1 [NCIt concept]

Keyword's position in hierarchy(ies) :

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