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DAW1

Chr 2q36.3

dynein assembly factor with WD repeats 1

Aliases:
FLJ25955, ODA16, DNAAF18
MANE:
ENST00000309931.3

Annotations refreshed 10 hours ago.

Predicted protein structure

Clinical relevance (Genomics England PanelApp)

Diagnostic Grade (Green)

  • DDG2P

    BIALLELIC, autosomal or pseudoautosomal
  • Fetal anomalies

    BIALLELIC, autosomal or pseudoautosomal
  • Laterality disorders and isomerism

    BIALLELIC, autosomal or pseudoautosomal
  • Non-CF bronchiectasis

    BIALLELIC, autosomal or pseudoautosomal
  • Respiratory ciliopathies including non-CF bronchiectasis

    BIALLELIC, autosomal or pseudoautosomal

Disease associations (Open Targets)

  • ciliary dyskinesia, primary, 52

    0.67
  • primary ciliary dyskinesia

    0.59
  • dementia

    0.38
  • allergic rhinitis

    0.38
  • asthma

    0.35
  • allergic disease

    0.34
  • Eczematoid dermatitis

    0.33
  • ovarian neoplasm

    0.28
  • childhood onset asthma

    0.27
  • adolescent idiopathic scoliosis

    0.27

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

Protein function (UniProt)

Dynein assembly factor with WD repeat domains 1

Required for axonemal dynein assembly and ciliary motility in ciliated organs, including Kupffer's vesicle, during embryogenesis (PubMed:36074124). Facilitates the onset of robust cilia motility during development (PubMed:36074124)

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.