WNT8B

Gene Information
 
Gene Symbol
WNT8B
 
Aliases
-
 
Entrez Gene ID
 
Gene Name
Wnt family member 8B
 
Chromosomal Location
10q24.31
 
HGNC ID
 
Summary
The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It encodes a protein which shows 95%, 86% and 71% amino acid identity to the mouse, zebrafish and Xenopus Wnt8B proteins, respectively. The expression patterns of the human and mouse genes appear identical and are restricted to the developing brain. The chromosomal location of this gene to 10q24 suggests it as a candidate gene for partial epilepsy. [provided by RefSeq, Jul 2008]
  e!Ensembl
Gene
Transcript  
Protein

Gene Ontology (GO)

GO ID Ontology Function Evidence Reference
GO:0007165 Biological process Signal transduction TAS 9536085
GO:0007369 Biological process Gastrulation ISS 7635061
GO:0007399 Biological process Nervous system development TAS 9536085
GO:0016055 Biological process Wnt signaling pathway IBA 21873635
GO:0030182 Biological process Neuron differentiation IBA 21873635
Protein Information
 
Protein Name
Protein Wnt-8b, epididymis secretory sperm binding protein, wingless-type MMTV integration site family, member 8B
 
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.
 
UniProt
 
Pfam
Pfam Accession Pfam ID
PF00110 wnt
Pathways
 
KEGG
 
Reactome
 

mTOR signaling pathway
Wnt signaling pathway
Hippo signaling pathway
Signaling pathways regulating pluripotency of stem cells
Melanogenesis
Cushing syndrome
Human papillomavirus infection
Pathways in cancer
Proteoglycans in cancer
Basal cell carcinoma
Breast cancer
Hepatocellular carcinoma
Gastric cancer

 

WNT ligand biogenesis and trafficking
Disassembly of the destruction complex and recruitment of AXIN to the membrane

     

Associated Diseases

Disease groupDisease NameReferences
Endocrine System Diseases
PCOS
Neoplasms
Gastrointestinal Cancer
Gastric Cancer
Medulloblastoma
Liver Cancer
References
 
 
PubMed ID Associated gene/s Associated condition Genetic Mutation Diagnostic Criteria Association with PCOS Ethnicity Conclusion
 
Endrometrial proliferation and development 
 
Rotterdam Criteria 
Direct 
18 PCOS patients and 8 control  
The considerable decrease in the expression of Wnt3, Wnt7a, and Wnt8b may be associated not only with lower endometrial thickness but also with sub-optimal endometrial development which likely is responsible for the poor pregnancy outcome due to the disturbance in estrogen signaling. 

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