TTC21B, tetratricopeptide repeat domain 21B, 79809

N. diseases: 76; N. variants: 24
Disease: Nephritis, Interstitial ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs140511594
rs140511594
Entrez Id: 79809;100506134
Gene Symbol: TTC21B;TTC21B-AS1
TTC21B;TTC21B-AS1
CUI: C0027707
Disease:
Nephritis, Interstitial 		0.010 GeneticVariation BEFREE Our results confirm the causal role of the homozygous p.P209L TTC21B mutation in two new families with FSGS and tubulointerstitial disease. 26940125 2017