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SLITRK6

Chr 13q31.1

SLIT and NTRK like family member 6

Aliases:
FLJ22774
MANE:
ENST00000647374.2

Annotations refreshed 9 hours ago.

Predicted protein structure

Clinical relevance (Genomics England PanelApp)

Diagnostic Grade (Green)

  • Monogenic hearing loss

    BIALLELIC, autosomal or pseudoautosomal

Disease associations (Open Targets)

  • high myopia-sensorineural deafness syndrome

    0.69
  • hearing loss, autosomal recessive

    0.39
  • Global developmental delay

    0.34
  • Hypercholesterolemia

    0.31
  • oligodendroglioma

    0.30
  • spinal stenosis

    0.28
  • schizophrenia

    0.28
  • urolithiasis

    0.26
  • celiac disease

    0.25
  • adolescent idiopathic scoliosis

    0.25

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

Protein function (UniProt)

SLIT and NTRK-like protein 6

Regulator of neurite outgrowth required for normal hearing and vision

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.