Figure 2 | Scientific Reports

Figure 2

From: Autosomal dominant tubulointerstitial kidney disease genotype and phenotype correlation in a Chinese cohort

Figure 2

Pedigree information of the families. Proband from family 3–13 had a positive family history of ADTKD. Black symbols denoted clinically affected individuals. Open symbols denoted clinically unaffected individuals. Gray symbols denoted family members with variants but no clinical symptoms. Arrow denoted the proband and below the proband symbol are the amino acid symbols. Family 3, family 12 and family 13 had variants in genes UMOD, REN, and HNF1B, respectively. For the family members which genetic testing was performed the results were listed below the symbol. MUT Family members carried the same clinically significant variant as the proband, WT Individuals without pathogenic variants.

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