Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5310
Gene Symbol: PKD1
PKD1
CUI: C1567435
Disease: Polycystic Kidney - body part
Polycystic Kidney - body part
0.350 Biomarker CTD_human Histone deacetylase 6 inhibition reduces cysts by decreasing cAMP and Ca2+ in knock-out mouse models of polycystic kidney disease. 28887310

2017

Entrez Id: 5310
Gene Symbol: PKD1
PKD1
CUI: C1567435
Disease: Polycystic Kidney - body part
Polycystic Kidney - body part
0.350 Biomarker CTD_human Therapeutic targeting of BET bromodomain protein, Brd4, delays cyst growth in ADPKD. 25877301

2015

Entrez Id: 5310
Gene Symbol: PKD1
PKD1
CUI: C1567435
Disease: Polycystic Kidney - body part
Polycystic Kidney - body part
0.350 Biomarker CTD_human Kidney-specific inactivation of the Pkd1 gene induces rapid cyst formation in developing kidneys and a slow onset of disease in adult mice. 17932118

2007

Entrez Id: 11231
Gene Symbol: SEC63
SEC63
CUI: C1567435
Disease: Polycystic Kidney - body part
Polycystic Kidney - body part
0.300 Biomarker CTD_human A genetic interaction network of five genes for human polycystic kidney and liver diseases defines polycystin-1 as the central determinant of cyst formation. 21685914

2011

Entrez Id: 5589
Gene Symbol: PRKCSH
PRKCSH
CUI: C1567435
Disease: Polycystic Kidney - body part
Polycystic Kidney - body part
0.300 Biomarker CTD_human A genetic interaction network of five genes for human polycystic kidney and liver diseases defines polycystin-1 as the central determinant of cyst formation. 21685914

2011

Entrez Id: 54903
Gene Symbol: MKS1
MKS1
CUI: C1567435
Disease: Polycystic Kidney - body part
Polycystic Kidney - body part
0.300 Biomarker GENOMICS_ENGLAND MKS1, encoding a component of the flagellar apparatus basal body proteome, is mutated in Meckel syndrome. 16415886

2006

Entrez Id: 54903
Gene Symbol: MKS1
MKS1
CUI: C1567435
Disease: Polycystic Kidney - body part
Polycystic Kidney - body part
0.300 Biomarker GENOMICS_ENGLAND MKS1, encoding a component of the flagellar apparatus basal body proteome, is mutated in Meckel syndrome. 16415886

2006

Entrez Id: 54903
Gene Symbol: MKS1
MKS1
CUI: C1567435
Disease: Polycystic Kidney - body part
Polycystic Kidney - body part
0.300 Biomarker GENOMICS_ENGLAND MKS1, encoding a component of the flagellar apparatus basal body proteome, is mutated in Meckel syndrome. 16415886

2006

Entrez Id: 169792
Gene Symbol: GLIS3
GLIS3
CUI: C1567435
Disease: Polycystic Kidney - body part
Polycystic Kidney - body part
0.300 Biomarker GENOMICS_ENGLAND Mutations in GLIS3 are responsible for a rare syndrome with neonatal diabetes mellitus and congenital hypothyroidism. 16715098

2006