Sequence Detail

ID/Version

Q923D5 Q3UMD8 O88539 Q8VDI0 (UniProt | EBI)

Last sequence update: 2005-09-13
Last annotation update: 2024-10-02

Sequence description from provider

RecName: Full=WW domain-binding protein 11; Short=WBP-11;AltName: Full=Splicing factor that interacts with PQBP-1 and PP1;

Provider

SWISS-PROT

Sequence

Polypeptide 641 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	Wbp11	WW domain binding protein 11	15	101	3	18

Sequence references in MGI

J:64694 Bedford MT, et al., WW domain-mediated interactions reveal a spliceosome-associated protein that binds a third class of proline-rich motif: the proline glycine and methionine-rich motif. Proc Natl Acad Sci U S A. 1998 Sep 1;95(18):10602-7
J:88011 Llorian M, et al., SIPP1, a novel pre-mRNA splicing factor and interactor of protein phosphatase-1. Biochem J. 2004 Feb 15;378(Pt 1):229-38
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:203468 Park J, et al., SIRT5-mediated lysine desuccinylation impacts diverse metabolic pathways. Mol Cell. 2013 Jun 27;50(6):919-30
J:292518 Huttlin EL, et al., A tissue-specific atlas of mouse protein phosphorylation and expression. Cell. 2010 Dec 23;143(7):1174-89
J:300837 Martin EMMA, et al., Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice. Hum Mol Genet. 2021 Jan 21;29(22):3662-3678