Skip to content
GenoLensGenoLens

FOSL2

Chr 2p23.2

FOS like 2, AP-1 transcription factor subunit

Aliases:
FRA2, FLJ23306
MANE:
ENST00000264716.9

Annotations refreshed 9 hours ago.

Predicted protein structure

Clinical relevance (Genomics England PanelApp)

Diagnostic Grade (Green)

  • Bilateral congenital or childhood onset cataracts

    MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
  • DDG2P

    MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
  • Ectodermal dysplasia

    MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
  • Fetal anomalies

    MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
  • Intellectual disability

    MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted

Disease associations (Open Targets)

  • aplasia cutis-enamel dysplasia syndrome

    0.72
  • hypertensive disorder

    0.48
  • hair color

    0.48
  • allergic rhinitis

    0.48
  • Crohn disease

    0.46
  • inflammatory bowel disease

    0.43
  • rosacea

    0.43
  • neurodegenerative disease

    0.41
  • Eczematoid dermatitis

    0.41
  • atopic eczema

    0.41

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

Protein function (UniProt)

Fos-related antigen 2

Controls osteoclast survival and size (By similarity). As a dimer with JUN, activates LIF transcription (By similarity). Activates CEBPB transcription in PGE2-activated osteoblasts (By similarity)

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.