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