Gene: IFT88 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 8100
Gene Symbol: IFT88
IFT88 		0.530 Biomarker disease BEFREE Indeed, hypomorphic mutations in the mouse ift88 (previously called Tg737) gene, which encodes a ciliogenic intraflagellar transport protein, result in malformation of primary cilia, and in the collecting ducts of kidney tubules this is accompanied by development of autosomal recessive polycystic kidney disease (PKD). 19276629 2009
Entrez Id: 8100
Gene Symbol: IFT88
IFT88 		0.530 Biomarker disease MGD Disruption of IFT results in both exocrine and endocrine abnormalities in the pancreas of Tg737(orpk) mutant mice. 15580285 2005
Entrez Id: 8100
Gene Symbol: IFT88
IFT88 		0.530 Biomarker disease MGD Orpk mouse model of polycystic kidney disease reveals essential role of primary cilia in pancreatic tissue organization. 15226261 2004
Entrez Id: 8100
Gene Symbol: IFT88
IFT88 		0.530 Biomarker disease MGD Loss of the Tg737 protein results in skeletal patterning defects. 12701101 2003
Entrez Id: 8100
Gene Symbol: IFT88
IFT88 		0.530 Biomarker disease MGD Phenotypic variations of orpk mutation and chromosomal localization of modifiers influencing kidney phenotype. 11773599 2001
Entrez Id: 8100
Gene Symbol: IFT88
IFT88 		0.530 Biomarker disease MGD Chlamydomonas IFT88 and its mouse homologue, polycystic kidney disease gene tg737, are required for assembly of cilia and flagella. 11062270 2000
Entrez Id: 8100
Gene Symbol: IFT88
IFT88 		0.530 GeneticVariation disease BEFREE Renal tubules are predisposed to cystogenesis when a germ line mutation is inherited in either the human PKD1 or PKD2 genes in autosomal dominant polycystic kidney disease (ADPKD) or when a homozygous mutation in Tg737 is inherited in the orpk mouse model of autosomal recessive polycystic kidney disease (ARPKD). 10200981 1999
Entrez Id: 8100
Gene Symbol: IFT88
IFT88 		0.530 Biomarker disease MGD Oval cell proliferation associated with the murine insertional mutation TgN737Rpw. 8952527 1996
Entrez Id: 8100
Gene Symbol: IFT88
IFT88 		0.530 GeneticVariation disease BEFREE Sequence analysis of the human hTg737 gene and its polymorphic sites in patients with autosomal recessive polycystic kidney disease. 8597639 1995
Entrez Id: 8100
Gene Symbol: IFT88
IFT88 		0.530 Biomarker disease CTD_human Insertional mutagenesis and molecular analysis of a new gene associated with polycystic kidney disease. 8608416 1995
Entrez Id: 8100
Gene Symbol: IFT88
IFT88 		0.530 Biomarker disease CTD_human Candidate gene associated with a mutation causing recessive polycystic kidney disease in mice. 8191288 1994
Entrez Id: 8100
Gene Symbol: IFT88
IFT88 		0.530 Biomarker disease MGD Candidate gene associated with a mutation causing recessive polycystic kidney disease in mice. 8191288 1994