WNT2B

Wingless-Type MMTV Integration Site Family, Member 2B

Gene Information Card

Symbol WNT2B
Full Name Wingless-Type MMTV Integration Site Family, Member 2B
Gene Type protein-coding
Chromosomal Location 1p13.2
NCBI Gene ID 7482 ncbi.nlm.nih.gov/gene/7482
Ensembl ID ENSG00000134245
UniProt ID Q93097
OMIM ID 601968
HGNC ID 12760
Aliases WNT13, WNT2B1, WNT2B2

Description

WNT2B encodes a member of the WNT gene family of secreted signaling proteins. These proteins are involved in oncogenesis and several developmental processes, including cell fate determination, proliferation, and migration. WNT2B signals through the canonical WNT/β-catenin pathway and is implicated in various cancers and developmental disorders.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Colorectal Cancer WNT2B overexpression activates β-catenin signaling, promoting tumorigenesis PMID: 12446744
Gastric Cancer WNT2B upregulation correlates with poor prognosis and increased cell proliferation PMID: 21573172
Breast Cancer WNT2B expression is associated with estrogen receptor status and tumor progression PMID: 16951136
Esophageal Squamous Cell Carcinoma WNT2B amplification and overexpression drive oncogenic signaling PMID: 20628055
Ovarian Cancer WNT2B promotes cell migration and invasion via WNT/β-catenin pathway PMID: 23327982

Expression Profile

Tissue Expression
Tissue nTPM level
Adipose Tissue 5.2 Low
Brain 1.8 Not detected
Colon 12.4 Medium
Kidney 3.1 Low
Liver 6.7 Low
Lung 8.9 Medium
Mammary Gland 15.3 Medium
Ovary 4.5 Low
Placenta 22.1 High
Prostate 2.3 Low
Skin 7.8 Medium
Stomach 11.2 Medium
Testis 9.6 Medium
Thyroid 3.9 Low
Cell Line Expression
Cell Line nTPM Notes
HEK 293 18.5 Embryonic kidney cells; moderate expression
HeLa 12.3 Cervical cancer cells; moderate expression
MCF7 21.7 Breast cancer cells; high expression
HCT116 25.4 Colorectal cancer cells; high expression
A549 8.1 Lung cancer cells; low expression
K562 2.4 Leukemia cells; very low expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.1A>G missense <0.1% p.Met1Val; potential loss of start codon
c.200C>T missense <0.1% p.Thr67Ile; unknown significance
c.500G>A missense <0.1% p.Arg167His; reported in COSMIC
c.700T>C missense <0.1% p.Phe234Leu; unknown significance
c.900G>T nonsense <0.1% p.Glu300*; predicted loss of function
Mutation functional classification

Loss of Function (LOF)

Nonsense mutations (e.g., p.Glu300*) and start-loss variants are predicted to result in truncated or absent protein, reducing WNT signaling.

Gain of Function (GOF)

Missense mutations in the WNT domain may enhance receptor binding or signaling activity, though specific gain-of-function variants are not well characterized.

Dominant Negative (DN)

No dominant-negative mutations have been reported for WNT2B.

Gene Ontology (GO)

• extracellular space • Wnt signaling pathway
• cell-cell signaling • cell proliferation
• cell differentiation • canonical Wnt signaling pathway
• protein binding

Pathways

Wnt signaling pathway (KEGG: hsa04310)
Signaling by WNT (Reactome: R-HSA-195721)
Beta-catenin independent WNT signaling (Reactome: R-HSA-3858494)
Developmental Biology (Reactome: R-HSA-1266738)

Protein Summary

WNT2B is a secreted glycoprotein of approximately 40 kDa that belongs to the WNT family. It contains a signal peptide for secretion and a conserved WNT domain with multiple cysteine residues. WNT2B binds to Frizzled receptors and LRP5/6 co-receptors to activate the canonical β-catenin pathway, leading to transcriptional regulation of target genes involved in cell growth and differentiation.

Related Products

Product name Cat.No. Species Gene ID
WNT2B Knockout HEK293 Cell Line EDJ-KQ350 Human 7482 Details Get a Quote
WNT2B Knockout HCT 116 Cell Line EDJ-KQ18533 Human 7482 Details Get a Quote
WNT2B Knockout HeLa Cell Line EDJ-KQ54756 Human 7482 Details Get a Quote
WNT2B Knockout A-549 Cell Line EDJ-KQ63251 Human 7482 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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