Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9742
Gene Symbol: IFT140
IFT140 		0.200 Biomarker disease MGD Cauli: a mouse strain with an Ift140 mutation that results in a skeletal ciliopathy modelling Jeune syndrome. 24009529 2013
Entrez Id: 9742
Gene Symbol: IFT140
IFT140 		0.200 Biomarker disease MGD Genome-wide ENU mutagenesis in combination with high density SNP analysis and exome sequencing provides rapid identification of novel mouse models of developmental disease. 23469164 2013
Entrez Id: 57539
Gene Symbol: WDR35
WDR35 		0.200 Biomarker disease MGD Human and mouse mutations in WDR35 cause short-rib polydactyly syndromes due to abnormal ciliogenesis. 21473986 2011
Entrez Id: 57560
Gene Symbol: IFT80
IFT80 		0.200 Biomarker disease MGD An Ift80 mouse model of short rib polydactyly syndromes shows defects in hedgehog signalling without loss or malformation of cilia. 21227999 2011
Entrez Id: 56916
Gene Symbol: SMARCAD1
SMARCAD1 		0.200 Biomarker disease MGD
Entrez Id: 79659
Gene Symbol: DYNC2H1
DYNC2H1 		0.200 Biomarker disease MGD