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WLS

Chr 1p31.3

Wnt ligand secretion mediator

Aliases:
FLJ23091, MRP, EVI, mig-14
MANE:
ENST00000262348.9

Annotations refreshed 9 hours ago.

Predicted protein structure

Clinical relevance (Genomics England PanelApp)

Diagnostic Grade (Green)

  • Fetal anomalies

    BIALLELIC, autosomal or pseudoautosomal
  • Severe microcephaly

    BIALLELIC, autosomal or pseudoautosomal
  • Structural eye disease

    BIALLELIC, autosomal or pseudoautosomal

Disease associations (Open Targets)

  • Zaki syndrome

    0.73
  • osteoporosis

    0.44
  • bone disorder

    0.43
  • open-angle glaucoma

    0.32
  • total hip arthroplasty

    0.30
  • osteoarthritis, hip

    0.30
  • Abnormality of the gastrointestinal tract

    0.29
  • glaucoma

    0.28
  • urolithiasis

    0.21
  • alcohol drinking

    0.21

Score is the Open Targets composite evidence score (0-1). Higher = stronger gene-disease association.

Protein function (UniProt)

Protein wntless homolog

Regulates Wnt proteins sorting and secretion in a feedback regulatory mechanism. This reciprocal interaction plays a key role in the regulation of expression, subcellular location, binding and organelle-specific association of Wnt proteins (PubMed:34587386). Plays also an important role in establishment of the anterior-posterior body axis formation during development (By similarity)

Data sources: HGNC (CC BY 4.0), AlphaFold (CC BY 4.0, Jumper et al. Nature 2021), Genomics England PanelApp (CC BY 4.0), ClinGen, Open Targets (CC0), UniProt.

Not for sole clinical decision-making. Always verify against primary sources.