Disease Annotation

Gene Info

  • Species: Human (Homo sapiens)
  • GeneID: 3861
  • Symbol: KRT14
  • Description: keratin 14

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Disease_Term Source Rank Other Values
Epidermolysis bullosa simplex, Koebner type, 131900 (3) OMIM high
  • Genome region : 12q13.13
  • Genome region : 17q21.2
  • OMIM_ID : 131900 OMIM phenotype ID
  • OMIM_ID : 148040 OMIM gene ID
  • OMIM_ID : 148066 OMIM gene ID
Epidermolysis bullosa simplex, recessive 1, 601001 (3) OMIM high
  • Genome region : 12q13.13
  • Genome region : 17q21.2
  • OMIM_ID : 148040 OMIM gene ID
  • OMIM_ID : 148066 OMIM gene ID
  • OMIM_ID : 601001 OMIM phenotype ID
Dermatopathia pigmentosa reticularis, 125595 (3) OMIM high
  • Genome region : 17q21.2
  • OMIM_ID : 125595 OMIM phenotype ID
  • OMIM_ID : 148066 OMIM gene ID
Epidermolysis bullosa simplex, Weber-Cockayne type, 131800 (3) OMIM high
  • Genome region : 12q13.13
  • Genome region : 17q21.2
  • OMIM_ID : 131800 OMIM phenotype ID
  • OMIM_ID : 148040 OMIM gene ID
  • OMIM_ID : 148066 OMIM gene ID
Epidermolysis bullosa simplex, Dowling-Meara type, 131760 (3) OMIM high
  • Genome region : 12q13.13
  • Genome region : 17q21.2
  • OMIM_ID : 131760 OMIM phenotype ID
  • OMIM_ID : 148040 OMIM gene ID
  • OMIM_ID : 148066 OMIM gene ID
Naegeli-Franceschetti-Jadassohn syndrome, 161000 (3) OMIM high
  • Genome region : 17q21.2
  • OMIM_ID : 148066 OMIM gene ID
  • OMIM_ID : 161000 OMIM phenotype ID