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ZNF407

Chr 18q23

zinc finger protein 407

Aliases:
FLJ20307, FLJ13839, KIAA1703
MANE:
ENST00000299687.10

Annotations refreshed 1 month ago.

Predicted protein structure

Clinical relevance (Genomics England PanelApp)

Moderate Evidence (Amber)

  • Intellectual disability

    BOTH monoallelic and biallelic, autosomal or pseudoautosomal
  • DDG2P

    BIALLELIC, autosomal or pseudoautosomal

Disease associations (Open Targets)

  • short stature, impaired intellectual development, microcephaly, hypotonia, and ocular anomalies

    0.45
  • nervous system benign neoplasm

    0.39
  • Neurodevelopmental delay

    0.33
  • substance abuse

    0.30
  • smoking behavior

    0.30
  • attention deficit-hyperactivity disorder

    0.30
  • smoking initiation

    0.30
  • Tietze syndrome

    0.28
  • breast disorder

    0.27
  • arterial embolism

    0.26

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

Protein function (UniProt)

Zinc finger protein 407

May be involved in transcriptional regulation

Curated MONDO disease pages that list ZNF407 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.