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WNT3

—Wnt Family Member 3

Chromosome: 17

Location: 17:46762506-46833154

OMIM: 165330

Ensembl: ENSG00000108379

Official·OMIM:165330 Official·ENSG00000108379

Encodes Wnt signaling pathway ligand. Mutations cause tetra-amelia syndrome.

Treatment Roadmap — WNT3

Preclinical

Phase 1

Phase 2

Phase 3

Approved

Clinical trials have approximately 10% success rate. This roadmap shows the current status, not guaranteed outcomes.

Associated Diseases

WNT3 No associated disease records found for this gene.

Summary

Clinical Trial

Approved Therapy

Registered Variant