Disease Annotation

Gene Info

  • Species:Human (Homo sapiens)
  • GeneID:182
  • Symbol:JAG1
  • Description:jagged canonical Notch ligand 1

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Disease_Term Source Rank Other Values
Tetralogy of Fallot, 187500 (3) OMIM high
  • Genome region :18q11.2
  • Genome region :19p13.11
  • Genome region :20p12.2
  • Genome region :22q11.21
  • Genome region :5q35.1
  • Genome region :8p23.1
  • Genome region :8q23.1
  • OMIM_ID :187500OMIM phenotype ID
  • OMIM_ID :600576OMIM gene ID
  • OMIM_ID :600584OMIM gene ID
  • OMIM_ID :601656OMIM gene ID
  • OMIM_ID :601920OMIM gene ID
  • OMIM_ID :602054OMIM gene ID
  • OMIM_ID :602880OMIM gene ID
  • OMIM_ID :603693OMIM gene ID
?Deafness, congenital heart defects, and posterior embryotoxon (3) OMIM high
  • Genome region :20p12.2
  • OMIM_ID :601920OMIM gene ID
Alagille syndrome 1, 118450 (3) OMIM high
  • Genome region :20p12.2
  • OMIM_ID :118450OMIM phenotype ID
  • OMIM_ID :601920OMIM gene ID
Blood pressure GWAS high
Systolic blood pressure GWAS high
Bone mineral density GWAS high
Cardiac hypertrophy GWAS high
Urinary bladder cancer GWAS high
Diastolic blood pressure GWAS high