Disease Annotation

Gene Info

  • Species:Human (Homo sapiens)
  • GeneID:4893
  • Symbol:NRAS
  • Description:NRAS proto-oncogene, GTPase

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Disease_Term Source Rank Other Values
Noonan syndrome 6, 613224 (3) OMIM high
  • Genome region :1p13.2
  • OMIM_ID :164790OMIM gene ID
  • OMIM_ID :613224OMIM phenotype ID
Epidermal nevus, somatic, 162900 (3) OMIM high
  • Genome region :1p13.2
  • OMIM_ID :162900OMIM phenotype ID
  • OMIM_ID :164790OMIM gene ID
Schimmelpenning-Feuerstein-Mims syndrome, somatic mosaic, 163200 (3) OMIM high
  • Genome region :11p15.5
  • Genome region :12p12.1
  • Genome region :1p13.2
  • OMIM_ID :163200OMIM phenotype ID
  • OMIM_ID :164790OMIM gene ID
  • OMIM_ID :190020OMIM gene ID
  • OMIM_ID :190070OMIM gene ID
Melanocytic nevus syndrome, congenital, somatic, 137550 (3) OMIM high
  • Genome region :1p13.2
  • OMIM_ID :137550OMIM phenotype ID
  • OMIM_ID :164790OMIM gene ID
Thyroid carcinoma, follicular, somatic, 188470 (3) OMIM high
  • Genome region :1p13.2
  • OMIM_ID :164790OMIM gene ID
  • OMIM_ID :188470OMIM phenotype ID
Colorectal cancer, somatic, 114500 (3) OMIM high
  • Genome region :14q24.3
  • Genome region :14q32.33
  • Genome region :15q15.1
  • Genome region :17p11.2
  • Genome region :17q24.1
  • Genome region :18q21.2
  • Genome region :19q13.33
  • Genome region :1p13.2
  • Genome region :22q13.2
  • Genome region :3p22.1
  • Genome region :3q26.32
  • Genome region :4p16.3
  • Genome region :5q22.2
  • Genome region :8p22
  • OMIM_ID :114500OMIM phenotype ID
  • OMIM_ID :116806OMIM gene ID
  • OMIM_ID :120470OMIM gene ID
  • OMIM_ID :134934OMIM gene ID
  • OMIM_ID :159350OMIM gene ID
  • OMIM_ID :164730OMIM gene ID
  • OMIM_ID :164790OMIM gene ID
  • OMIM_ID :171834OMIM gene ID
  • OMIM_ID :600040OMIM gene ID
  • OMIM_ID :602700OMIM gene ID
  • OMIM_ID :602860OMIM gene ID
  • OMIM_ID :604025OMIM gene ID
  • OMIM_ID :604258OMIM gene ID
  • OMIM_ID :604395OMIM gene ID
  • OMIM_ID :604584OMIM gene ID
  • OMIM_ID :607273OMIM gene ID
  • OMIM_ID :611731OMIM gene ID
Neurocutaneous melanosis, somatic, 249400 (3) OMIM high
  • Genome region :1p13.2
  • OMIM_ID :164790OMIM gene ID
  • OMIM_ID :249400OMIM phenotype ID
?RAS-associated autoimmune lymphoproliferative syndrome type IV, somatic, 614470 (3) OMIM high
  • Genome region :1p13.2
  • OMIM_ID :164790OMIM gene ID
  • OMIM_ID :614470OMIM phenotype ID
Autism GWAS high