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
Phospholipid levels (plasma) GWAS high
Rheumatoid arthritis GWAS high
Immune response to smallpox vaccine (IL-6) GWAS high
Preeclampsia GWAS high
Esophageal cancer GWAS high
middle facial morphology traits (quantitative measurement) GWAS high
Psoriasis GWAS high
Esophageal squamous cell carcinoma GWAS high