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GenoLensGenoLens

NTNG2

Chr 9q34.13

netrin G2

Aliases:
KIAA1857, Lmnt2, NetrinG2
MANE:
ENST00000393229.4

Annotations refreshed 9 hours ago.

Predicted protein structure

Clinical relevance (Genomics England PanelApp)

Diagnostic Grade (Green)

  • DDG2P

    BIALLELIC, autosomal or pseudoautosomal
  • Intellectual disability

    BIALLELIC, autosomal or pseudoautosomal

Disease associations (Open Targets)

  • neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia

    0.75
  • neurodevelopmental disorder

    0.39
  • complex neurodevelopmental disorder

    0.37
  • Global developmental delay

    0.34
  • Areflexia

    0.33
  • Generalized hypotonia

    0.33
  • Stereotypical hand wringing

    0.33
  • urolithiasis

    0.29
  • alcohol drinking

    0.29
  • Achalasia

    0.28

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

Protein function (UniProt)

Netrin-G2

Involved in controlling patterning and neuronal circuit formation at the laminar, cellular, subcellular and synaptic levels. Promotes neurite outgrowth of both axons and dendrites

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.