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RRAS2

Chr 11p15.2

RAS related 2

Aliases:
TC21
MANE:
ENST00000256196.9

Annotations refreshed 1 month 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, imprinted status unknown
  • Monogenic short stature

    MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
  • RASopathies

    MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
  • Familial breast cancer

    Unknown
  • Inherited ovarian cancer (without breast cancer)

    Unknown

Disease associations (Open Targets)

  • Noonan syndrome

    0.78
  • noonan syndrome 12

    0.69
  • hereditary disease

    0.46
  • neurodegenerative disease

    0.46
  • ovarian cancer

    0.45
  • vitamin D deficiency

    0.43
  • vitamin deficiency disorder

    0.42
  • endometrial cancer

    0.40
  • hypertrophic cardiomyopathy

    0.39
  • breast ductal adenocarcinoma

    0.37

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

Protein function (UniProt)

Ras-related protein R-Ras2

GTP-binding protein with GTPase activity, involved in the regulation of MAPK signaling pathway and thereby controlling multiple cellular processes (PubMed:31130282, PubMed:31130285, PubMed:39809765). Regulates craniofacial development (PubMed:31130282, PubMed:31130285)

Curated MONDO disease pages that list RRAS2 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.