Disease Annotation

Gene Info

  • Species: Human (Homo sapiens)
  • GeneID: 861
  • Symbol: RUNX1
  • Description: RUNX family transcription factor 1

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Disease_Term Source Rank Other Values
Platelet disorder, familial, with associated myeloid malignancy, 601399 (3) OMIM high
  • Genome region : 21q22.12
  • OMIM_ID : 151385 OMIM gene ID
  • OMIM_ID : 601399 OMIM phenotype ID
Leukemia, acute myeloid, 601626 (3) OMIM high
  • Genome region : 10p12.31
  • Genome region : 12p12.1
  • Genome region : 21q22.12
  • Genome region : 3q27-q28
  • Genome region : 4q12
  • Genome region : 8p11.23
  • OMIM_ID : 151385 OMIM gene ID
  • OMIM_ID : 164920 OMIM gene ID
  • OMIM_ID : 190070 OMIM gene ID
  • OMIM_ID : 600700 OMIM gene ID
  • OMIM_ID : 601626 OMIM phenotype ID
  • OMIM_ID : 602409 OMIM gene ID
  • OMIM_ID : 607083 OMIM gene ID
Preeclampsia GWAS high
Esophageal cancer GWAS high
middle facial morphology traits (quantitative measurement) GWAS high
Psoriasis GWAS high
Esophageal squamous cell carcinoma GWAS high
Phospholipid levels (plasma) GWAS high
Rheumatoid arthritis GWAS high
Immune response to smallpox vaccine (IL-6) GWAS high