Skip to content
GenoLensGenoLens

HFM1

Chr 1p22.2

helicase for meiosis 1

Aliases:
MER3, FLJ39011, FLJ36760
MANE:
ENST00000370425.8

Annotations refreshed 9 hours ago.

Predicted protein structure

Clinical relevance (Genomics England PanelApp)

Diagnostic Grade (Green)

  • Primary ovarian insufficiency

    BIALLELIC, autosomal or pseudoautosomal

Disease associations (Open Targets)

  • primary ovarian failure

    0.55
  • genetic non-acquired premature ovarian failure

    0.40
  • neurodegenerative disease

    0.40
  • Azoospermia

    0.34
  • diabetes mellitus

    0.28
  • obesity disorder

    0.26
  • bone Paget disease

    0.26
  • stomach disorder

    0.26
  • limb injury

    0.25
  • liver disorder

    0.25

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

Protein function (UniProt)

Probable ATP-dependent DNA helicase HFM1

Required for crossover formation and complete synapsis of homologous chromosomes during meiosis

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.