Disease Annotation

Gene Info

  • Species: Human (Homo sapiens)
  • GeneID: 9927
  • Symbol: MFN2
  • Description: mitofusin 2

Marrvel Logo and Link

Export (tab separated) Export to Excel

Disease_Term Source Rank Other Values
Hereditary motor and sensory neuropathy VIA, 601152 (3) OMIM high
  • Genome region : 1p36.22
  • OMIM_ID : 601152 OMIM phenotype ID
  • OMIM_ID : 608507 OMIM gene ID
Charcot-Marie-Tooth disease, axonal, type 2A2A, 609260 (3) OMIM high
  • Genome region : 1p36.22
  • OMIM_ID : 608507 OMIM gene ID
  • OMIM_ID : 609260 OMIM phenotype ID
Charcot-Marie-Tooth disease, axonal, type 2A2B, 617087 (3) OMIM high
  • Genome region : 1p36.22
  • OMIM_ID : 608507 OMIM gene ID
  • OMIM_ID : 617087 OMIM phenotype ID
Inflammatory skin disease GWAS high
Platelet count GWAS high