TTC8 protein, human

Preferred Label : TTC8 protein, human;

MeSH note : homozygous null BBS8 mutation leads to Bardet-Biedl syndrome with randomization of left-right body axis symmetry, a known defect of the nodal cilium; RefSeq NM_144596;

MeSH synonym : Bardet- Biedl syndrome 8 protein, human; tetratricopeptide repeat domain 8 protein, human; TPR repeat protein 8, human; BBS8 protein, human;

Is substance : O;

Details

Origin ID

C478138;

UMLS CUI

C1312472;

MeSH indexing information
- bardet-biedl syndrome [MeSH Descriptor]
MeSH term(s) associated for indexing
- cytoskeletal proteins [MeSH Descriptor]
- proteins [MeSH Descriptor]
Record concept(s)
- TTC8 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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