Disease Annotation

Gene Info

  • Species:Human (Homo sapiens)
  • GeneID:3643
  • Symbol:INSR
  • Description:insulin receptor

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Disease_Term Source Rank Other Values
Leprechaunism, 246200 (3) OMIM high
  • Genome region :19p13.2
  • OMIM_ID :147670OMIM gene ID
  • OMIM_ID :246200OMIM phenotype ID
Hyperinsulinemic hypoglycemia, familial, 5, 609968 (3) OMIM high
  • Genome region :19p13.2
  • OMIM_ID :147670OMIM gene ID
  • OMIM_ID :609968OMIM phenotype ID
Rabson-Mendenhall syndrome, 262190 (3) OMIM high
  • Genome region :19p13.2
  • OMIM_ID :147670OMIM gene ID
  • OMIM_ID :262190OMIM phenotype ID
Diabetes mellitus, insulin-resistant, with acanthosis nigricans, 610549 (3) OMIM high
  • Genome region :19p13.2
  • OMIM_ID :147670OMIM gene ID
  • OMIM_ID :610549OMIM phenotype ID
Triglycerides GWAS high
Height GWAS high
Polycystic ovary syndrome GWAS high
Asthma (childhood onset) GWAS high
Urate levels GWAS high
Hypothyroidism GWAS high
Thyroid hormone levels GWAS high
Diabetic retinopathy GWAS high