Gene content    
WNT5A ( by HUGO)
Wingless-Type MMTV Integration Site Family, Member 5A
Tumor suppressor gene
Wingless-Type MMTV Integration Site Family
Member 5A
WNT-5A Protein
hWNT5A
Protein Wnt-5a
NCBI: 3p21-p14    Ensembl: 3p14.3
WNT5A_HUMANSize: 380 amino acidsMass: 42339 Da

  • Subunit: Homooligomer; disulfide-linked, leading to inactivation. Interacts with PORCN. Interacts with WLS (By similarity)
  • Tissue specificity: Expression is increased in differentiated thyroid carcinomas compared to normal thyroid tissue and anaplastic thyroid tumors where expression is low or undetectable. Expression is found in thyrocytes but not in stromal cells (at protein level) [IMAGE] Pat
  • Function:
    UniProtKB/Swiss-Prot Summary: WNT5A_HUMAN, P41221 Function: Ligand for members of the frizzled family of seven transmembrane receptors. Can activate or inhibit canonical Wnt signaling, depending on receptor context. In the presence of FZD4, activates beta-catenin signaling. In the presence of ROR2, inhibits the canonical Wnt pathway by promoting beta-catenin degradation through a GSK3-independent pathway which involves down-regulation of beta-catenin-induced reporter gene expression. Suppression of the canonical pathway allows chondrogenesis to occur and inhibits tumor formation. Stimulates cell migration. Decreases proliferation, migration, invasiveness and clonogenicity of carcinoma cells and may act as a tumor suppressor. Mediates motility of melanoma cells. Required during embryogenesis for extension of the primary anterior-posterior axis and for outgrowth of limbs and the genital tubercle. Inhibits type II collagen expression in chondrocytes
  • Similarity:
    Belongs to the Wnt family [IMAGE]
  • Protein Domain/Family    
    Source ID Domain Name Type
    InterProIPR005817WntWnt superfamilyFamily
    BlocksIPB005816Secreted growth factor Wnt proteinSecreted growth factor Wnt protein

    Gene Ontology    
    Type Term Evidence Source Pub
    Biological Process cellular protein localization IDA GOA 19177143
    cellular response to calcium ion IEP GOA 18703641
    cellular response to interferon-gamma IEP GOA 18174455
    cellular response to lipopolysaccharide IEP GOA 18174455
    cellular response to transforming growth factor beta stimulus IEP GOA 15040835
    embryonic skeletal system development IMP GOA 19918918
    epithelial to mesenchymal transition IEP GOA 12841867
    face development IMP GOA 19918918
    genitalia development IMP GOA 19918918
    hematopoietic stem cell proliferation IDA GOA 9787155
    keratinocyte differentiation IEP GOA 19399181
    lens development in camera-type eye ISS GOA 16258938
    male gonad development IEP GOA 17848411
    negative regulation of apoptotic process IDA GOA 19251946
    negative regulation of canonical Wnt signaling pathway IDA GOA 17976063
    negative regulation of canonical Wnt signaling pathway IGI GOA 12952940
    negative regulation of mesenchymal cell proliferation IDA GOA 19878652
    negative regulation of transcription, DNA-templated IDA GOA 19277043
    optic cup formation involved in camera-type eye development ISS GOA 16258938
    palate development IMP GOA 18413325
    positive regulation of angiogenesis IMP GOA 17035633
    positive regulation of cGMP metabolic process IDA GOA 19946729
    positive regulation of chemokine biosynthetic process IMP GOA 19520808
    positive regulation of cytokine secretion involved in immune response IMP GOA 18174455
    positive regulation of endothelial cell migration IMP GOA 17035633
    positive regulation of endothelial cell proliferation IMP GOA 17986384
    positive regulation of fibroblast proliferation IDA GOA 19251946
    positive regulation of inflammatory response IMP GOA 18174455
    positive regulation of interleukin-1 beta secretion IMP GOA 18174455
    positive regulation of interleukin-6 production IMP GOA 18174455
    positive regulation of macrophage activation IMP GOA 18174455
    positive regulation of macrophage cytokine production IMP GOA 18174455
    positive regulation of NF-kappaB transcription factor activity IDA GOA 18287027
    positive regulation of protein catabolic process IGI GOA 12952940
    positive regulation of protein kinase C signaling IMP GOA 19099253
    positive regulation of response to cytokine stimulus IDA GOA 19399181
    positive regulation of T cell chemotaxis IMP GOA 19520808
    positive regulation of transcription from RNA polymerase II promoter IMP GOA 18174455
    positive regulation of transcription, DNA-templated IMP GOA 19847889
    positive regulation of type I interferon-mediated signaling pathway IDA GOA 19399181
    response to organic substance IEP GOA 17486081
    Wnt signaling pathway, calcium modulating pathway IMP GOA 17986384
    Wnt signaling pathway, calcium modulating pathway IDA GOA 19946729
    wound healing IDA GOA 19878652
    Cellular Component extracellular space IDA GOA 18703641
    Molecular Function frizzled binding IPI GOA 18174455
    receptor agonist activity IC GOA 18174455
    receptor tyrosine kinase-like orphan receptor binding IPI GOA 18287027
    sequence-specific DNA binding transcription factor activity IMP GOA 19847889
    transcription regulatory region DNA binding IDA GOA 19847889

    Disorder & Mutation    
    Source Disease
    SWISS-PROTRobinow syndrome autosomal dominant (DRS) [MIM:180700]: A disease characterized by short-limb dwarfism, costovertebral segmentation defects and abnormalities of the head, face and external genitalia. The clinical signs are generally milder in dominant cases. Note=The disease is caused by mutations affecting the gene represented in this entry

    WNT5A cross reference    
    PubMed OMIM Entrez Gene NCKU SNP Nucleotide UniProt Genome Data Viewer HomoloGene