Skip to content
GenoLensGenoLens

WIPF1

Chr 2q31.1

WAS/WASL interacting protein family member 1

Aliases:
WIP
MANE:
ENST00000679041.1

Annotations refreshed 9 hours ago.

Predicted protein structure

Clinical relevance (Genomics England PanelApp)

Diagnostic Grade (Green)

  • COVID-19 research

    BIALLELIC, autosomal or pseudoautosomal
  • Cytopenia - NOT Fanconi anaemia

    BIALLELIC, autosomal or pseudoautosomal
  • Cytopenias and congenital anaemias

    BIALLELIC, autosomal or pseudoautosomal
  • Primary immunodeficiency or monogenic inflammatory bowel disease

    BIALLELIC, autosomal or pseudoautosomal

Disease associations (Open Targets)

  • Wiskott-Aldrich syndrome

    0.66
  • atrial fibrillation

    0.49
  • Abnormality of the skeletal system

    0.42
  • atrial flutter

    0.38
  • Increased blood pressure

    0.31
  • osteonecrosis

    0.29
  • hypertensive disorder

    0.26
  • chronic obstructive pulmonary disease

    0.26
  • cardiac arrhythmia

    0.26
  • cardiovascular disorder

    0.25

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

Protein function (UniProt)

WAS/WASL-interacting protein family member 1

Plays a role in the reorganization of the actin cytoskeleton. Contributes with NCK1 and GRB2 in the recruitment and activation of WASL. May participate in regulating the subcellular localization of WASL, resulting in the disassembly of stress fibers in favor of filopodia formation. Plays a role in the formation of cell ruffles (By similarity). Plays an important role in the intracellular motility of vaccinia virus by functioning as an adapter for recruiting WASL to vaccinia virus

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.