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NRAS

Chr 1p13.2

NRAS proto-oncogene, GTPase

Aliases:
N-ras
MANE:
ENST00000369535.5

Annotations refreshed 1 month ago.

Predicted protein structure

Clinical relevance (Genomics England PanelApp)

Diagnostic Grade (Green)

  • Adult solid tumours cancer susceptibility

    MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
  • Childhood solid tumours cancer susceptibility

    MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
  • DDG2P

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

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

    MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
  • Intellectual disability

    MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
  • IUGR and IGF abnormalities

    MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
  • Monogenic short stature

    MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted

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Disease associations (Open Targets)

  • Noonan syndrome

    0.83
  • Noonan syndrome 6

    0.81
  • large congenital melanocytic nevus

    0.71
  • nevus, epidermal

    0.70
  • acute myeloid leukemia

    0.70
  • autoimmune lymphoproliferative syndrome type 4

    0.68
  • melanoma

    0.68
  • cancer

    0.65
  • juvenile myelomonocytic leukemia

    0.64
  • plasma cell myeloma

    0.64

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

Protein function (UniProt)

GTPase NRas

Signal transducer in the Ras-MAPK signaling pathway that regulates cell proliferation and survival (PubMed:30712867). Ras proteins bind GDP/GTP and possess intrinsic GTPase activity (PubMed:30712867). Recognized by LZTR1 that mediates its ubiquitination by a BCR (BTB-CUL3-RBX1) E3 ubiquitin-protein ligase complex (PubMed:40934300)

Curated MONDO disease pages that list NRAS among their top associated genes.

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.