Disease Annotation

Gene Info

  • Species: Human (Homo sapiens)
  • GeneID: 7466
  • Symbol: WFS1
  • Description: wolframin ER transmembrane glycoprotein

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Disease_Term Source Rank Other Values
Wolfram syndrome, 222300 (3) OMIM high
  • Genome region : 4p16.1
  • OMIM_ID : 222300 OMIM phenotype ID
  • OMIM_ID : 606201 OMIM gene ID
?Cataract 41, 116400 (3) OMIM high
  • Genome region : 4p16.1
  • OMIM_ID : 116400 OMIM phenotype ID
  • OMIM_ID : 606201 OMIM gene ID
Wolfram-like syndrome, autosomal dominant, 614296 (3) OMIM high
  • Genome region : 4p16.1
  • OMIM_ID : 606201 OMIM gene ID
  • OMIM_ID : 614296 OMIM phenotype ID
{Diabetes mellitus, noninsulin-dependent, association with}, 125853 (3) OMIM high
  • Genome region : 4p16.1
  • OMIM_ID : 125853 OMIM phenotype ID
  • OMIM_ID : 606201 OMIM gene ID
Deafness, autosomal dominant 6/14/38, 600965 (3) OMIM high
  • Genome region : 4p16.1
  • OMIM_ID : 600965 OMIM phenotype ID
  • OMIM_ID : 606201 OMIM gene ID
Type 2 diabetes GWAS high
Type 2 diabetes and other traits GWAS high