InnateDB Protein
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IDBP-55693.5
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Last Modified
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2014-10-13 [Report errors or provide feedback]
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Gene Symbol
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WNT3
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Protein Name
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wingless-type MMTV integration site family, member 3
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Synonyms
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INT4;
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Species
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Homo sapiens
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Ensembl Protein
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ENSP00000225512
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InnateDB Gene
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IDBG-55691 (WNT3)
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Protein Structure
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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}.
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Subcellular Localization |
Secreted, extracellular space, extracellular matrix.
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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.
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Tissue Specificity |
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Comments |
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Number of Interactions
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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]
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Protein-Protein |
1
[view]
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Protein-DNA |
0
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Protein-RNA |
0
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DNA-DNA |
1
[view]
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RNA-RNA |
0
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DNA-RNA |
0
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Predicted by orthology |
Total |
5 [view]
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Molecular Function |
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Biological Process |
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Cellular Component |
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PDB ID |
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InterPro |
IPR005817
Wnt
IPR009141
Wnt-3 protein
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PFAM |
PF00110
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PRINTS |
PR01349
PR01843
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PIRSF |
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SMART |
SM00097
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TIGRFAMs |
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Modification |
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SwissProt |
P56703
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PhosphoSite |
PhosphoSite-P56703
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TrEMBL |
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UniProt Splice Variant |
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Entrez Gene |
7473
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UniGene |
Hs.606555
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RefSeq |
NP_110380
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HUGO |
HGNC:12782
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OMIM |
165330
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CCDS |
CCDS11505
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HPRD |
01318
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IMGT |
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EMBL |
AB067628
AY009397
BC112116
BC112118
BC114219
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GenPept |
AAG38657
AAI12117
AAI12119
AAI14220
BAB70502
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