Gene: TTC8 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 123016
Gene Symbol: TTC8
TTC8 		0.340 Biomarker disease BEFREE Loss of Bardet-Biedl syndrome protein-8 (BBS8) perturbs olfactory function, protein localization, and axon targeting. 21646512 2011
Entrez Id: 123016
Gene Symbol: TTC8
TTC8 		0.340 Biomarker disease MGD To explore the nature of olfactory defects in BBS, a genetic ablation of the mouse Bbs8 gene that incorporates a fluorescent reporter protein was created. 21646512 2011
Entrez Id: 123016
Gene Symbol: TTC8
TTC8 		0.340 Biomarker disease BEFREE This study confirms the small role of BBS7 and TTC8 in the overall mutational load of BBS patients. 19402160 2009
Entrez Id: 123016
Gene Symbol: TTC8
TTC8 		0.340 GeneticVariation disease BEFREE Mutations in BBS8 probably account for only a minority of BBS families (2%), underlining the difficulty of genotyping heterogeneous conditions. 16308660 2006
Entrez Id: 123016
Gene Symbol: TTC8
TTC8 		0.340 GeneticVariation disease LHGDN In one family, a homozygous null BBS8 mutation leads to BBS with randomization of left-right body axis symmetry, a known defect of the nodal cilium. 14520415 2003
Entrez Id: 123016
Gene Symbol: TTC8
TTC8 		0.340 GeneticVariation disease BEFREE In one family, a homozygous null BBS8 mutation leads to BBS with randomization of left-right body axis symmetry, a known defect of the nodal cilium. 14520415 2003
Entrez Id: 123016
Gene Symbol: TTC8
TTC8 		0.340 CausalMutation disease CLINVAR