Details for: Wbp11

Gene ID: 60321

Symbol: Wbp11

Ensembl ID: ENSMUSG00000030216

Description: WW domain binding protein 11

Associated with

Other Information

Genular Protein ID: 2645618859

Symbol: WBP11_MOUSE

Name: WW domain-binding protein 11

UniProtKB Accession Codes:

Q923D5 O88539 Q3UMD8 Q8VDI0

Database IDs:

AGR 1 AlphaFoldDB 1 Bgee 1 BioGRID 1 BioGRID-ORCS 1 CCDS 1 CTD 1 ChiTaRS 1 DNASU 1 ELM 1 EMBL 6 EPD 1 Ensembl 1 ExpressionAtlas 1 GO 11 GeneTree 1 Genevisible 1 GlyGen 1 HOGENOM 1 InParanoid 1 IntAct 1 InterPro 1 KEGG 1 MGI 1 MINT 1 MaxQB 1 NCBI Taxonomy 1 OMA 1 OrthoDB 1 PANTHER 2 PRO 1 PaxDb 1 Pfam 1 PhosphoSitePlus 1 PhylomeDB 1 Proteomes 1 ProteomicsDB 1 Pumba 1 RNAct 1 Reactome 1 RefSeq 2 SAM 1 SMR 1 STRING 1 TreeFam 1 UCSC 1 UniProtKB 1 VEuPathDB 1 eggNOG 1 iPTMnet 1 jPOST 1

Citations:

PubMed ID: 16141072

Title: The transcriptional landscape of the mammalian genome.

PubMed ID: 16141072

DOI: 10.1126/science.1112014

PubMed ID: 15489334

Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).

PubMed ID: 15489334

DOI: 10.1101/gr.2596504

PubMed ID: 9724750

Title: 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.

PubMed ID: 9724750

DOI: 10.1073/pnas.95.18.10602

PubMed ID: 14640981

Title: SIPP1, a novel pre-mRNA splicing factor and interactor of protein phosphatase-1.

PubMed ID: 14640981

DOI: 10.1042/bj20030950

PubMed ID: 16162498

Title: Nucleocytoplasmic shuttling of the splicing factor SIPP1.

PubMed ID: 16162498

DOI: 10.1074/jbc.m509185200

PubMed ID: 17242355

Title: Large-scale phosphorylation analysis of mouse liver.

PubMed ID: 17242355

DOI: 10.1073/pnas.0609836104

PubMed ID: 21183079

Title: A tissue-specific atlas of mouse protein phosphorylation and expression.

PubMed ID: 21183079

DOI: 10.1016/j.cell.2010.12.001

PubMed ID: 23806337

Title: SIRT5-mediated lysine desuccinylation impacts diverse metabolic pathways.

PubMed ID: 23806337

DOI: 10.1016/j.molcel.2013.06.001

PubMed ID: 33276377

Title: Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice.

PubMed ID: 33276377

DOI: 10.1093/hmg/ddaa258

Sequence Information:

  • Length: 641
  • Mass: 69875
  • Checksum: 9C97281B4257B1F6
  • Sequence:
    • MGRRSTSSTK SGKFMNPTDQ ARKEARKREL KKNKKQRMMV RAAVLKMKDP KQIIRDMEKL 
DEMEFNPVQQ PQLNEKVLKD KRKKLRETFE RILRLYEKEN PDIYKELRKL EVEYEQKRAQ 
LSQYFDAVKN AQHVEVESIP LPDMPHAPSN ILIQDIPLPG AQPPSILKKT SAYGPPARAV 
SILPLLGHGV PRLPPGRKPP GPPPGPPPPQ VLQMYGRKVG FALDLPPRRR DEDMLYSPEL 
AQRGHDDDMS STSEDDGYPE DMDQDKHDDS TEDSDTDRSD AESDGDEFGH REDSERDNTE 
EKKSGLSVRF ADMPGKSRKK KKNMKELTPL QAMMLRMAGQ EIPEEGREVE EFSEEEDADD 
SDDSEAEKQS QKQHKDDGHS DSTAAASSQQ QAPPQSAPAS QIQAPPMPGP PPLGPPPAPP 
LRPPGPPTGL PPGPPPGAPP FLRPPGMPGI RGPLPRLLPP GPPPGRPPGP PPGPPPGLPP 
GPPPRGPPPR LPPPAPPGIP PPRPGMMRPP LVPPLGPAPP GLFPPAPLPN PGVLSAPPSL 
IQRPKADDAS AATIEKKATA TISAKPQITN PKAEVTRFVP TALRVRRENK GATAVPQRRS 
EDDSAVPVAK AAPRSGPSVA VSVQTKDDVY EAFMKEMEGL L

Database document:

This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.