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ZNF668

Chr 16p11.2

zinc finger protein 668

Aliases:
FLJ13479
MANE:
ENST00000300849.5

Annotations refreshed 9 hours ago.

Predicted protein structure

Clinical relevance (Genomics England PanelApp)

Diagnostic Grade (Green)

  • Fetal anomalies

    BIALLELIC, autosomal or pseudoautosomal
  • Intellectual disability

    BIALLELIC, autosomal or pseudoautosomal
  • Monogenic short stature

    BIALLELIC, autosomal or pseudoautosomal
  • Severe microcephaly

    BIALLELIC, autosomal or pseudoautosomal

Disease associations (Open Targets)

  • neurodevelopmental disorder with poor growth, large ears, and dysmorphic facies

    0.65
  • Failure to thrive

    0.42
  • Profound global developmental delay

    0.42
  • Progressive microcephaly

    0.42
  • Severe short-limb dwarfism

    0.33
  • neurodegenerative disease

    0.27
  • Abnormality of the skeletal system

    0.18
  • atrial fibrillation

    0.14
  • myoepithelial tumor

    0.11
  • mathematical ability

    0.10

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

Protein function (UniProt)

Zinc finger protein 668

May be involved in transcriptional regulation. May play a role in DNA repair process

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.