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FRYL

Chr 4p11

FRY like transcription coactivator

Aliases:
DKFZp686E205, AF4p12, MOR2
MANE:
ENST00000358350.9

Annotations refreshed 9 hours ago.

Predicted protein structure

Clinical relevance (Genomics England PanelApp)

Diagnostic Grade (Green)

  • DDG2P

    MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
  • Fetal anomalies

    MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
  • Intellectual disability

    MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted

Disease associations (Open Targets)

  • Pan-Chung-Bellen syndrome

    0.66
  • type 2 diabetes mellitus

    0.26
  • migraine disorder

    0.26
  • dementia

    0.24
  • thrombophilia

    0.20
  • menopause

    0.13
  • nephronophthisis

    0.08
  • Abnormality of the skeletal system

    0.08
  • posterior cortical atrophy

    0.08
  • familial idiopathic steroid-resistant nephrotic syndrome

    0.08

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

Protein function (UniProt)

Protein furry homolog-like

Plays a key role in maintaining the integrity of polarized cell extensions during morphogenesis, regulates the actin cytoskeleton and plays a key role in patterning sensory neuron dendritic fields by promoting avoidance between homologous dendrites as well as by limiting dendritic branching (By similarity). May function as a 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.