Homo sapiens Protein: WNT8B
Summary
InnateDB Protein IDBP-86501.4
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol WNT8B
Protein Name wingless-type MMTV integration site family, member 8B
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000340677
InnateDB Gene IDBG-86499 (WNT8B)
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. {ECO:0000269PubMed:9536085}.
Subcellular Localization Secreted, extracellular space, extracellular matrix.
Disease Associations
Tissue Specificity Expression is restricted to the brain, and more specifically to the forebrain. {ECO:0000269PubMed:9536085}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
GO:0005102 receptor binding
GO:0005109 frizzled binding
Biological Process
GO:0007165 signal transduction
GO:0007275 multicellular organismal development
GO:0007369 gastrulation
GO:0007399 nervous system development
GO:0010628 positive regulation of gene expression
GO:0010629 negative regulation of gene expression
GO:0016055 Wnt signaling pathway
GO:0030182 neuron differentiation
GO:0032355 response to estradiol
GO:0032526 response to retinoic acid
GO:0045165 cell fate commitment
GO:0048263 determination of dorsal identity
GO:0071300 cellular response to retinoic acid
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 Q93098
PhosphoSite PhosphoSite-
TrEMBL
UniProt Splice Variant
Entrez Gene 7479
UniGene Hs.421281
RefSeq NP_003384
HUGO HGNC:12789
OMIM 601396
CCDS CCDS7494
HPRD 03235
IMGT
EMBL AB073637 AL133352 AL359759 X91940 Y11094 Y11108
GenPept BAB83924 CAA63017 CAA71968 CAA71994 CAH71991 CAH73565