MeSH Browser

MeSH Supplementary: TTC8 protein, human
Unique ID: C478138
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C478138
Entry Term(s): BBS8 protein, human; Bardet- Biedl syndrome 8 protein, human; TPR repeat protein 8, human; tetratricopeptide repeat domain 8 protein, human
Registry Number: 0
Previous Indexing: *Proteins (2003-2020)
Heading Mapped to: *Cytoskeletal Proteins
Frequency: 15
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
Source: Nature 2003 Oct 9;425(6958);628-33
Indexing Information: Bardet-Biedl Syndrome
Date of Entry: 2003/10/24
Revision Date: 2020/01/08

TTC8 protein, human MeSH Supplementary Concept Data 2024