Version 5.4
Bos taurus Protein: BT.101628
Summary
InnateDB Protein IDBP-684399.2
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol BT.101628
Protein Name wingless-type MMTV integration site family, member 1
Synonyms
Species Bos taurus
Ensembl Protein ENSBTAP00000020414
InnateDB Gene IDBG-632755 (BT.101628)
Protein Structure
UniProt Annotation
Function
Subcellular Localization
Disease Associations
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 14 interaction(s) predicted by orthology.
Predicted by orthology
Total 14 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005102 receptor binding
GO:0005109 frizzled binding
GO:0005125 cytokine activity
GO:0005515 protein binding
GO:0019904 protein domain specific binding
GO:0044212 transcription regulatory region DNA binding
Biological Process
GO:0000578 embryonic axis specification
GO:0001658 branching involved in ureteric bud morphogenesis
GO:0001934 positive regulation of protein phosphorylation
GO:0007267 cell-cell signaling
GO:0007275 multicellular organismal development
GO:0007520 myoblast fusion
GO:0008284 positive regulation of cell proliferation
GO:0009611 response to wounding
GO:0010592 positive regulation of lamellipodium assembly
GO:0010812 negative regulation of cell-substrate adhesion
GO:0014902 myotube differentiation
GO:0016055 Wnt signaling pathway
GO:0021527 spinal cord association neuron differentiation
GO:0021536 diencephalon development
GO:0021551 central nervous system morphogenesis
GO:0021588 cerebellum formation
GO:0021797 forebrain anterior/posterior pattern specification
GO:0022004 midbrain-hindbrain boundary maturation during brain development
GO:0022037 metencephalon development
GO:0022408 negative regulation of cell-cell adhesion
GO:0030182 neuron differentiation
GO:0030512 negative regulation of transforming growth factor beta receptor signaling pathway
GO:0030514 negative regulation of BMP signaling pathway
GO:0030579 ubiquitin-dependent SMAD protein catabolic process
GO:0030901 midbrain development
GO:0030917 midbrain-hindbrain boundary development
GO:0033077 T cell differentiation in thymus
GO:0042472 inner ear morphogenesis
GO:0042770 signal transduction in response to DNA damage
GO:0043568 positive regulation of insulin-like growth factor receptor signaling pathway
GO:0044336 canonical Wnt signaling pathway involved in negative regulation of apoptotic process
GO:0045165 cell fate commitment
GO:0045596 negative regulation of cell differentiation
GO:0045599 negative regulation of fat cell differentiation
GO:0045747 positive regulation of Notch signaling pathway
GO:0045893 positive regulation of transcription, DNA-templated
GO:0045944 positive regulation of transcription from RNA polymerase II promoter
GO:0048146 positive regulation of fibroblast proliferation
GO:0048663 neuron fate commitment
GO:0048664 neuron fate determination
GO:0051091 positive regulation of sequence-specific DNA binding transcription factor activity
GO:0060061 Spemann organizer formation
GO:0060070 canonical Wnt signaling pathway
GO:0060348 bone development
GO:0061184 positive regulation of dermatome development
GO:0071425 hematopoietic stem cell proliferation
GO:0090344 negative regulation of cell aging
GO:2000059 negative regulation of protein ubiquitination involved in ubiquitin-dependent protein catabolic process
Cellular Component
GO:0005576 extracellular region
GO:0005578 proteinaceous extracellular matrix
GO:0005615 extracellular space
GO:0005737 cytoplasm
GO:0009986 cell surface
Protein Structure and Domains
PDB ID
InterPro IPR005817 Wnt
IPR009139 Wnt-1 protein
PFAM PF00110
PRINTS PR01349
PR01841
PIRSF
SMART SM00097
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt
PhosphoSite PhosphoSite-
TrEMBL E1BEN9
UniProt Splice Variant
Entrez Gene 540662
UniGene Bt.101628
RefSeq NP_001107663
HUGO
OMIM
CCDS
HPRD
IMGT
EMBL DAAA02012953
GenPept

If you use InnateDB for your research, please cite the following publication:

Breuer et al., InnateDB: systems biology of innate immunity and beyond - recent updates and continuing curation. Nucl. Acids Res. (2013) 41 (D1) 

InnateDB is being developed jointly by the Brinkman Laboratory (Simon Fraser University, British Columbia, Canada), the Hancock Laboratory (University of British Columbia, Vancouver, British Columbia) and the Lynn EMBL Australia Group (South Australian Health & Medical Research Institute and Flinders University, Adelaide, Australia).

Funding is currently provided by Allergen and EMBL Australia. Previous funding has been provided by Genome Canada, the Foundation for the National Institutes of Health through the Grand Challenges in Global Health initiative and by Teagasc. InnateDB curated interactions are licensed under the Design Science License. All other data is licensed under the terms of the originating database. Contact: innatedb-mail@sfu.ca