Sequence Detail

ID/Version

Q8VD72 Q9DCP7 (UniProt | EBI)

Last sequence update: 2002-03-01
Last annotation update: 2025-02-05

Sequence description from provider

RecName: Full=Tetratricopeptide repeat protein 8; Short=TPR repeat protein 8;AltName: Full=Bardet-Biedl syndrome 8 protein homolog;

Provider

SWISS-PROT

Sequence

Polypeptide 515 aa

Source

Organism mouse

See UniProt | EBI for source

Annotated genes and markers

Follow the symbol links to get more information on the GO terms, expression assays, orthologs, phenotypic alleles, and other information for the genes or markers below.

Type	Symbol	Name	GO Terms	Expression Assays	Orthologs	Phenotypic Alleles
Gene	Ttc8	tetratricopeptide repeat domain 8	62	99	3	10

Sequence references in MGI

J:85975 Ansley SJ, et al., Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome. Nature. 2003 Oct 9;425(6958):628-33
J:99680 The FANTOM Consortium and RIKEN Genome Exploration Research Group and Genome Science Group (Genome Network Project Core Group), The Transcriptional Landscape of the Mammalian Genome. Science. 2005;309(5740):1559-1563
J:177990 Seo S, et al., A Novel Protein LZTFL1 Regulates Ciliary Trafficking of the BBSome and Smoothened. PLoS Genet. 2011 Nov;7(11):e1002358
J:233668 Broekhuis JR, et al., Regulation of cilium length and intraflagellar transport by the RCK-kinases ICK and MOK in renal epithelial cells. PLoS One. 2014;9(9):e108470