Skip to content
GenoLensGenoLens

ZFX

Chr Xp22.11

zinc finger protein X-linked

Aliases:
ZNF926
MANE:
ENST00000304543.10

Annotations refreshed 10 hours 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)
  • Fetal anomalies

    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, syndromic 37

    0.64
  • neoplasm

    0.10
  • hepatocellular carcinoma

    0.10
  • non-small cell lung carcinoma

    0.10
  • chronic myelogenous leukemia, BCR-ABL1 positive

    0.08
  • colorectal carcinoma

    0.08
  • renal cell carcinoma

    0.08
  • breast cancer

    0.07
  • breast carcinoma

    0.07
  • cancer

    0.07

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

Protein function (UniProt)

Zinc finger X-chromosomal protein

Probable transcriptional activator

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.