Skip to content
GenoLensGenoLens

ZMYM3

Chr Xq13.1

zinc finger MYM-type containing 3

Aliases:
ZNF198L2, DXS6673E, KIAA0385, MYM
MANE:
ENST00000314425.9

Annotations refreshed 1 month ago.

Predicted protein structure

Clinical relevance (Genomics England PanelApp)

Diagnostic Grade (Green)

  • DDG2P

    X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
  • Intellectual disability

    X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)

Disease associations (Open Targets)

  • intellectual developmental disorder, X-linked 112

    0.63
  • prostate adenocarcinoma

    0.56
  • neurodegenerative disease

    0.34
  • medulloblastoma

    0.28
  • B-cell chronic lymphocytic leukemia

    0.25
  • lung adenocarcinoma

    0.22
  • neurodevelopmental disorder

    0.22
  • head and neck squamous cell carcinoma

    0.21
  • lung carcinoma

    0.20
  • small cell lung carcinoma

    0.20

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

Protein function (UniProt)

Zinc finger MYM-type protein 3

Required for regulation of cell morphology and cytoskeletal organization

Curated MONDO disease pages that list ZMYM3 among their top associated genes.

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.