Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 79809
Gene Symbol: TTC21B
TTC21B
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases 		0.420 GeneticVariation BEFREE We identified a novel TTC21B mutation demonstrating that p.P209L is not the unique causative mutation of this nephropathy. 26940125

2017
Entrez Id: 79809
Gene Symbol: TTC21B
TTC21B
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases 		0.420 GeneticVariation BEFREE Altogether, these data suggest that this homozygous TTC21B p.P209L mutation leads to a novel hereditary kidney disorder with both glomerular and tubulointerstitial damages. 24876116

2014
Entrez Id: 79809
Gene Symbol: TTC21B
TTC21B
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases 		0.420 Biomarker CTD_human TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum. 21258341

2011
Entrez Id: 79809
Gene Symbol: TTC21B
TTC21B
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases 		0.420 Biomarker HPO