Disease Annotation

Gene Info

  • Species: Human (Homo sapiens)
  • GeneID: 3265
  • Symbol: HRAS
  • Description: HRas proto-oncogene, GTPase

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Disease_Term Source Rank Other Values
Costello syndrome, 218040 (3) OMIM high
  • Genome region : 11p15.5
  • OMIM_ID : 190020 OMIM gene ID
  • OMIM_ID : 218040 OMIM phenotype ID
{Spitz nevus or nevus spilus, somatic}, 137550 (3) OMIM high
  • Genome region : 11p15.5
  • OMIM_ID : 137550 OMIM phenotype ID
  • OMIM_ID : 190020 OMIM 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 : 163200 OMIM phenotype ID
  • OMIM_ID : 164790 OMIM gene ID
  • OMIM_ID : 190020 OMIM gene ID
  • OMIM_ID : 190070 OMIM gene ID
{Thyroid carcinoma, follicular, somatic}, 188470 (3) OMIM high
  • Genome region : 11p15.5
  • OMIM_ID : 188470 OMIM phenotype ID
  • OMIM_ID : 190020 OMIM gene ID
{Bladder cancer, somatic}, 109800 (3) OMIM high
  • Genome region : 11p15.5
  • OMIM_ID : 109800 OMIM phenotype ID
  • OMIM_ID : 190020 OMIM gene ID
Congenital myopathy with excess of muscle spindles, 218040 (3) OMIM high
  • Genome region : 11p15.5
  • OMIM_ID : 190020 OMIM gene ID
  • OMIM_ID : 218040 OMIM phenotype ID
{Nevus sebaceous or woolly hair nevus, somatic}, 162900 (3) OMIM high
  • Genome region : 11p15.5
  • OMIM_ID : 162900 OMIM phenotype ID
  • OMIM_ID : 190020 OMIM gene ID