Gene: IFT172 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 26160
Gene Symbol: IFT172
IFT172 		0.110 GeneticVariation disease BEFREE IFT172 is a member of the IFT complex B, and IFT172 mutation is associated with pathologies including short rib thoracic dysplasia, retinitis pigmentosa and Bardet-Biedl syndrome, but how it underpins these conditions is not clear. 31850339 2019
Entrez Id: 26160
Gene Symbol: IFT172
IFT172 		0.110 Biomarker disease HPO