Disease Annotation

Gene Info

  • Species:Human (Homo sapiens)
  • GeneID:169522
  • Symbol:KCNV2
  • Description:potassium voltage-gated channel modifier subfamily V member 2

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Disease_Term Source Rank Other Values
Retinal cone dystrophy 3B, 610356 (3) OMIM high
  • Genome region :9p24.2
  • OMIM_ID :607604OMIM gene ID
  • OMIM_ID :610356OMIM phenotype ID
Alzheimer's disease (age of onset) GWAS high
Vascular endothelial growth factor levels GWAS high
Blood trace element (Se levels) GWAS high
Obesity-related traits GWAS high