Disease Annotation

Gene Info

  • Species: Human (Homo sapiens)
  • GeneID: 3785
  • Symbol: KCNQ2
  • Description: potassium voltage-gated channel subfamily Q member 2

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Disease_Term Source Rank Other Values
Seizures, benign neonatal, 1, 121200 (3) OMIM high
  • Genome region : 20q13.33
  • OMIM_ID : 121200 OMIM phenotype ID
  • OMIM_ID : 602235 OMIM gene ID
Epileptic encephalopathy, early infantile, 7, 613720 (3) OMIM high
  • Genome region : 20q13.33
  • OMIM_ID : 602235 OMIM gene ID
  • OMIM_ID : 613720 OMIM phenotype ID
Myokymia, 121200 (3) OMIM high
  • Genome region : 20q13.33
  • OMIM_ID : 121200 OMIM phenotype ID
  • OMIM_ID : 602235 OMIM gene ID