Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 79809
Gene Symbol: TTC21B
TTC21B 		0.700 CausalMutation disease CLINVAR Contribution of the TTC21B gene to glomerular and cystic kidney diseases. 26940125 2017
Entrez Id: 79809
Gene Symbol: TTC21B
TTC21B 		0.700 Biomarker disease GENOMICS_ENGLAND A homozygous missense mutation in the ciliary gene TTC21B causes familial FSGS. 24876116 2014
Entrez Id: 79809
Gene Symbol: TTC21B
TTC21B 		0.700 CausalMutation disease CLINVAR A homozygous missense mutation in the ciliary gene TTC21B causes familial FSGS. 24876116 2014
Entrez Id: 79809
Gene Symbol: TTC21B
TTC21B 		0.700 GeneticVariation disease UNIPROT Mutations in C5ORF42 cause Joubert syndrome in the French Canadian population. 22425360 2012
Entrez Id: 79809
Gene Symbol: TTC21B
TTC21B 		0.700 GeneticVariation disease UNIPROT TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum. 21258341 2011
Entrez Id: 79809
Gene Symbol: TTC21B
TTC21B 		0.700 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 79809
Gene Symbol: TTC21B
TTC21B 		0.700 Biomarker disease CTD_human
Entrez Id: 100506134
Gene Symbol: TTC21B-AS1
TTC21B-AS1 		0.100 CausalMutation disease CLINVAR Contribution of the TTC21B gene to glomerular and cystic kidney diseases. 26940125 2017
Entrez Id: 100506134
Gene Symbol: TTC21B-AS1
TTC21B-AS1 		0.100 CausalMutation disease CLINVAR A homozygous missense mutation in the ciliary gene TTC21B causes familial FSGS. 24876116 2014