Gene: IFT27 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 11020
Gene Symbol: IFT27
IFT27 		0.420 CausalMutation disease CLINVAR Identification and Characterization of Known Biallelic Mutations in the IFT27 (BBS19) Gene in a Novel Family With Bardet-Biedl Syndrome. 30761183 2019
Entrez Id: 11020
Gene Symbol: IFT27
IFT27 		0.420 GeneticVariation disease BEFREE The phenotype in patients with IFT27 gene variants is wide ranging from Bardet-Biedl syndrome to a lethal phenotype. 29704304 2018
Entrez Id: 11020
Gene Symbol: IFT27
IFT27 		0.420 GeneticVariation disease BEFREE IFT27, encoding a small GTPase component of IFT particles, is mutated in a consanguineous family with Bardet-Biedl syndrome. 24488770 2014
Entrez Id: 11020
Gene Symbol: IFT27
IFT27 		0.420 GermlineCausalMutation disease ORPHANET IFT27, encoding a small GTPase component of IFT particles, is mutated in a consanguineous family with Bardet-Biedl syndrome. 24488770 2014