Homo sapiens Protein: WNT8A
Summary
InnateDB Protein IDBP-232306.7
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol WNT8A
Protein Name wingless-type MMTV integration site family, member 8A
Synonyms WNT8D;
Species Homo sapiens
Ensembl Protein ENSP00000381739
InnateDB Gene IDBG-46500 (WNT8A)
Protein Structure
UniProt Annotation
Function Ligand for members of the frizzled family of seven transmembrane receptors. May play an important role in the development and differentiation of certain forebrain structures, notably the hippocampus.
Subcellular Localization Secreted, extracellular space, extracellular matrix.
Disease Associations
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Experimentally validated
Total 1 [view]
Protein-Protein 1 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005102 receptor binding
GO:0005109 frizzled binding
GO:0048018 receptor agonist activity
Biological Process
GO:0007275 multicellular organismal development
GO:0014034 neural crest cell fate commitment
GO:0016055 Wnt signaling pathway
GO:0030182 neuron differentiation
GO:0032526 response to retinoic acid
GO:0044324 regulation of transcription involved in anterior/posterior axis specification
GO:0044335 canonical Wnt receptor signaling pathway involved in neural crest cell differentiation
GO:0060021 palate development
GO:0060070 canonical Wnt signaling pathway
GO:0061317 canonical Wnt receptor signaling pathway involved in cardiac muscle cell fate commitment
Cellular Component
GO:0005576 extracellular region
GO:0005578 proteinaceous extracellular matrix
GO:0005615 extracellular space
Protein Structure and Domains
PDB ID
InterPro IPR005817 Wnt
IPR013301 Wnt-8 protein
PFAM PF00110
PRINTS PR01349
PR01892
PIRSF
SMART SM00097
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q9H1J5
PhosphoSite PhosphoSite-Q9H1J5
TrEMBL
UniProt Splice Variant
Entrez Gene 7478
UniGene Hs.591274
RefSeq NP_490645
HUGO HGNC:12788
OMIM 606360
CCDS CCDS43368
HPRD 05898
IMGT
EMBL AB057725 AY009402
GenPept AAG38662 BAB60960