Homo sapiens Protein: WNT3
Summary
InnateDB Protein IDBP-55693.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol WNT3
Protein Name wingless-type MMTV integration site family, member 3
Synonyms INT4;
Species Homo sapiens
Ensembl Protein ENSP00000225512
InnateDB Gene IDBG-55691 (WNT3)
Protein Structure
UniProt Annotation
Function Ligand for members of the frizzled family of seven transmembrane receptors. Wnt-3 and Wnt-3a play distinct roles in cell-cell signaling during morphogenesis of the developing neural tube (By similarity). {ECO:0000250}.
Subcellular Localization Secreted, extracellular space, extracellular matrix.
Disease Associations Tetraamelia, autosomal recessive (ARTTRA) [MIM:273395]: A rare human genetic disorder characterized by complete absence of all four limbs and other anomalies such as craniofacial, nervous system, pulmonary, skeletal and urogenital defects. {ECO:0000269PubMed:14872406}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 2 experimentally validated interaction(s) in this database.
They are also associated with 5 interaction(s) predicted by orthology.
Experimentally validated
Total 2 [view]
Protein-Protein 1 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 1 [view]
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 5 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005102 receptor binding
GO:0005109 frizzled binding
GO:0005515 protein binding
GO:0019904 protein domain specific binding
GO:0048018 receptor agonist activity
Biological Process
GO:0000902 cell morphogenesis
GO:0001707 mesoderm formation
GO:0007275 multicellular organismal development
GO:0007276 gamete generation
GO:0007411 axon guidance
GO:0009948 anterior/posterior axis specification
GO:0009950 dorsal/ventral axis specification
GO:0009952 anterior/posterior pattern specification
GO:0010628 positive regulation of gene expression
GO:0016055 Wnt signaling pathway
GO:0030182 neuron differentiation
GO:0035115 embryonic forelimb morphogenesis
GO:0035116 embryonic hindlimb morphogenesis
GO:0044338 canonical Wnt receptor signaling pathway involved in mesenchymal stem cell differentiation
GO:0044339 canonical Wnt receptor signaling pathway involved in osteoblast differentiation
GO:0045165 cell fate commitment
GO:0048646 anatomical structure formation involved in morphogenesis
GO:0048697 positive regulation of collateral sprouting in absence of injury
GO:0048843 negative regulation of axon extension involved in axon guidance
GO:0060064 Spemann organizer formation at the anterior end of the primitive streak
GO:0060070 canonical Wnt signaling pathway
GO:0060173 limb development
GO:0060174 limb bud formation
GO:0060323 head morphogenesis
GO:0061180 mammary gland epithelium development
GO:0071300 cellular response to retinoic acid
Cellular Component
GO:0005576 extracellular region
GO:0005578 proteinaceous extracellular matrix
GO:0005615 extracellular space
GO:0005737 cytoplasm
GO:0005788 endoplasmic reticulum lumen
GO:0005796 Golgi lumen
GO:0005886 plasma membrane
GO:0031012 extracellular matrix
Protein Structure and Domains
PDB ID
InterPro IPR005817 Wnt
IPR009141 Wnt-3 protein
PFAM PF00110
PRINTS PR01349
PR01843
PIRSF
SMART SM00097
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt P56703
PhosphoSite PhosphoSite-P56703
TrEMBL
UniProt Splice Variant
Entrez Gene 7473
UniGene Hs.606555
RefSeq NP_110380
HUGO HGNC:12782
OMIM 165330
CCDS CCDS11505
HPRD 01318
IMGT
EMBL AB067628 AY009397 BC112116 BC112118 BC114219
GenPept AAG38657 AAI12117 AAI12119 AAI14220 BAB70502