WNT5A (Wnt Family Member 5A) is a Protein Coding gene. Diseases associated with WNT5A include Robinow Syndrome, Autosomal Dominant 1 and Robinow Syndrome. Among its related pathways are Presynaptic function of Kainate receptors and HTLV-I infection. Gene Ontology (GO) annotations related to this gene include DNA binding transcription factor activity and protein domain specific binding. An important paralog of this gene is WNT5B.
Related Pathway/CSCs feature
 Niche WNT5A regulates the actin cytoskeleton during regeneration of hematopoietic stem cells.
J Exp Med.2017 Jan;214(1):165-181. [ 27998927 ]
 WNT5A is a key regulator of the epithelial-mesenchymal transition and cancer stem cell properties in human gastric carcinoma cells.
Pathobiology.2013;80(5):235-44. [ 23615002 ]