Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5314
Gene Symbol: PKHD1
PKHD1
Autosomal Recessive Polycystic Kidney Disease
1.000 GeneticVariation LHGDN Since the misregulation of Ca(2+) signaling may lead to aberrant structure and function of the collecting ducts in kidney of rat with ARPKD, present study aimed to investigate the further mechanisms of abnormal proliferation of cystic cells by inhibition of PKHD1 expression. 17669261

2007

Entrez Id: 5314
Gene Symbol: PKHD1
PKHD1
Autosomal Recessive Polycystic Kidney Disease
1.000 GeneticVariation LHGDN In fact, cholangiocytes isolated from an ARPKD rat model develop shorter and dysmorphic cilia, suggesting polyductin to be important for normal ciliary morphology. 17160262

2006

Entrez Id: 5314
Gene Symbol: PKHD1
PKHD1
Autosomal Recessive Polycystic Kidney Disease
1.000 AlteredExpression LHGDN Mutations of HNF-1beta produce congenital cystic abnormalities of the kidney, and previous studies showed that HNF-1beta regulates the expression of the autosomal recessive polycystic kidney disease (ARPKD) gene, Pkhd1. 15647252

2005

Entrez Id: 5314
Gene Symbol: PKHD1
PKHD1
Autosomal Recessive Polycystic Kidney Disease
1.000 GeneticVariation LHGDN Screening for major genomic PKHD1 rearrangements will further improve mutation analysis in ARPKD. 16199545

2005

Entrez Id: 5314
Gene Symbol: PKHD1
PKHD1
Autosomal Recessive Polycystic Kidney Disease
1.000 GeneticVariation LHGDN A novel gene encoding a TIG multiple domain protein is a positional candidate for autosomal recessive polycystic kidney disease. 12079288

2002

Entrez Id: 5314
Gene Symbol: PKHD1
PKHD1
Autosomal Recessive Polycystic Kidney Disease
1.000 GeneticVariation LHGDN A mutation was characterized in the rat and screening the 66 coding exons of the human ortholog (PKHD1) in 14 probands with ARPKD revealed 6 truncating and 12 missense mutations; 8 of the affected individuals were compound heterozygotes. 11919560

2002