10.35092/yhjc.12040620.v1
Michael Levine
Michael
Levine
Rebecca J. Gordon
Rebecca J.
Gordon
Dong Li
Dong
Li
Joshua Zaritsky
Joshua
Zaritsky
Daniel Doyle
Daniel
Doyle
Supplemental Figure for “Digenic Heterozygous Mutations in SLC34A3 and SLC34A1 Cause Dominant Hypophosphatemic Rickets with Hypercalciuria”
The NIH Figshare Archive
2020
Digenic inheritance
Rickets, hypophosphatemic
Nephrolithiasis
2020-03-27 19:02:28
Figure
https://nih.figshare.com/articles/figure/Supplemental_Figure_for_Digenic_Heterozygous_Mutations_in_SLC34A3_and_SLC34A1_Cause_Dominant_Hypophosphatemic_Rickets_with_Hypercalciuria_/12040620
<div>Supplemental Figure for “Digenic Heterozygous Mutations in SLC34A3 and SLC34A1 Cause Dominant Hypophosphatemic Rickets with Hypercalciuria”</div><div><br></div><div>Supplemental Figure 1. Sanger sequencing of SLC34A3 and rs28434439 alternative alleles.</div><div><br></div><div>Sanger sequencing of subcloned DNA fragments showing mutant (A) and wild type (B) alleles, demonstrating that the SLC34A3 mutant allele and the rs28434439 alternative allele are not linked together (Panels A through H). PCR sequences from subject III-6 shows heterozygosity (T/C) for rs28434439 (Panel I) indicating presence of paternal wild type allele (A), and by extension, confirming the maternal origin of mutant SLC34A3 allele. These observations confirm the imputation results that the shared haplotype between father and mother carries the SLC34A3 mutation.</div>