Disease Annotation

Gene Info

  • Species:Human (Homo sapiens)
  • GeneID:1763
  • Symbol:DNA2
  • Description:DNA replication helicase/nuclease 2

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Disease_Term Source Rank Other Values
?Seckel syndrome 8, 615807 (3) OMIM high
  • Genome region :10q21.3
  • OMIM_ID :601810OMIM gene ID
  • OMIM_ID :615807OMIM phenotype ID
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 6, 615156 (3) OMIM high
  • Genome region :10q21.3
  • OMIM_ID :601810OMIM gene ID
  • OMIM_ID :615156OMIM phenotype ID