Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3872
Gene Symbol: KRT17
KRT17 		0.780 GeneticVariation disease BEFREE Missense mutations in keratin 17 cause either pachyonychia congenita type 2 or a phenotype resembling steatocystoma multiplex. 9008238 1997
Entrez Id: 3872
Gene Symbol: KRT17
KRT17 		0.780 GeneticVariation disease UNIPROT Missense mutations in keratin 17 cause either pachyonychia congenita type 2 or a phenotype resembling steatocystoma multiplex. 9008238 1997
Entrez Id: 3872
Gene Symbol: KRT17
KRT17 		0.780 GeneticVariation disease UNIPROT Keratin 16 and keratin 17 mutations cause pachyonychia congenita. 7539673 1995
Entrez Id: 3872
Gene Symbol: KRT17
KRT17 		0.780 Biomarker disease GENOMICS_ENGLAND Eruptive vellus hair cyst and steatocystoma multiplex in a patient with pachyonychia congenita. 8288793 1994
Entrez Id: 3872
Gene Symbol: KRT17
KRT17 		0.780 CausalMutation disease CLINVAR
Entrez Id: 3872
Gene Symbol: KRT17
KRT17 		0.780 Biomarker disease CTD_human
Entrez Id: 3868
Gene Symbol: KRT16
KRT16 		0.500 Biomarker disease MGD
Entrez Id: 3868
Gene Symbol: KRT16
KRT16 		0.500 Biomarker disease CTD_human
Entrez Id: 3854
Gene Symbol: KRT6B
KRT6B 		0.310 GeneticVariation disease BEFREE It has been demonstrated that PC-2 is caused by mutations in the keratin 17 and keratin 6b genes. 16620218 2006
Entrez Id: 3854
Gene Symbol: KRT6B
KRT6B 		0.310 Biomarker disease CTD_human
Entrez Id: 3853
Gene Symbol: KRT6A
KRT6A 		0.300 Biomarker disease CTD_human
Entrez Id: 4193
Gene Symbol: MDM2
MDM2 		0.010 Biomarker disease BEFREE The apoptotic cells in PC-2/swtp53 and PC-2/swtp53/pCMV-neo cell lines were 12.1%-12.9%, while the double transfected cell line, PC-2/swtp53/pCMV-MDM2, showed less (3.2%) apoptotic cells than its parent cell lines. 11263374 1998