Tctn1 protein, human

Preferred Label : Tctn1 protein, human;

MeSH note : mutation leads to Joubert syndrome; RefSeq NM_001082538;

MeSH synonym : tectonic1 protein, human;

Is substance : O;

Details

Origin ID

C561486;

UMLS CUI

C3252201;

MeSH term(s) associated for indexing
- membrane proteins [MeSH Descriptor]
Record concept(s)
- Tctn1 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)
- Tectonic-1 [NCIt concept]

Keyword's position in hierarchy(ies) :

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