Mutations in 329 probands with suspected renal electrolyte disorders
Renan E. AparicioiD, Sheng Chih JiniD, Weilai DongiD, Samir ZaidiiD, Michael C. SierantiD, James KnightiD, Robert D. Bjornson, Christopher CastaldiiD, Shrikant ManeiD, Thomas M. Kaneko, Carol J. Nelson-WilliamsiD, Richard P. LiftoniD
Abstract
The spectrum of coding and non-coding of mutations that contribute to Mendelian diseases is largely unknown. This question is broadly relevant to molecular diagnostic efforts in real-world settings, particularly when the scope of biochemical and other tests performed may be limited prior to genetic testing. We report the results of whole exome sequencing of DNA from 329 patients referred by physicians for suspicion of genetic causes of renal electrolyte disorders, predominantly featuring hypokalemia and/or hypomagnesemia with normal to low blood pressure. 295 probands were found to have known/likely disease-causing genotypes; these included 254 with biallelic mutations in one of 9 genes known to cause salt wasting, and 34 with monoallelic mutations in these same genes. Seven other probands had mutations in genes known to cause renal hypomagnesemia. Among these, 197 probands had biallelic or monoallelic (n = 7) damaging variants in the Gitelman syndrome (GS) gene SLC12A3, which encodes the Na-Cl cotransporter of the distal convoluted tubule. WGS sequencing in the 7 monoallelic probands, who all had pathognomonic electrolyte values for GS, identified two deep intronic variants that introduced splice sites producing frameshifting mutations, a small exonic deletion missed by WES, and a novel deep intronic variant of unknown function. Thus non-coding variation (outside exons and flanking splice sites) accounted for only two likely disease-related variants among 400 GS alleles, with 4 other alleles unexplained after WGS. Among patients with isolated hypomagnesemia, six had monoallelic deletions in HNF1B. Additionally, a novel homoplasmic mitochondrial isoleucine tRNA variant was associated with hypomagnesemia and depression/anxiety in seven relatives spanning three generations who shared a maternal lineage. The electrolyte profiles of probands with disease-associated genotypes were consistent with the paradigmatic features associated with mutation in each gene.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 0
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- mTOR-activating mutations in RRAGD cause kidney tubulopathy and cardiomyopathy (KICA) syndrome
Karl P. Schlingmann, François Jouret, … Jeroen H. F. de Baaij·bioRxiv·Mar 11, 2021
- Genome mining yields new disease-associated ROMK variants with distinct defects
Nga H. Nguyen, Srikant Sarangi, … Jeffrey L. Brodsky·PLoS GeneticsPeer-reviewed·Nov 13, 2023
- Identification and functional characterization of two novel mutations in KCNJ10 and PI4KB in SeSAME syndrome without electrolyte imbalance
Ravi Kumar Nadella, Anirudh S. Chellappa, … Ramakrishnan Kannan·Human GenomicsPeer-reviewed·Oct 22, 2019
- GWAS of serum ALT and AST reveals an association of SLC30A10 Thr95Ile with hypermanganesemia symptoms
Lucas D. Ward, Ho-Chou Tu, … Paul Nioi·Nature CommunicationsPeer-reviewed·Jul 27, 2021
- ATP7B Variant c.1934T>G p.Met645Arg Causes Wilson Disease by Promoting Exon 6 Skipping
Daniele Merico, Carl Spickett, … Brendan J. Frey·npj Genomic MedicinePeer-reviewed·Apr 8, 2020
- Comprehensive screening shows that mutations in the known syndromic genes are rare in individuals presenting with hyperinsulinaemic hypoglycaemia
Thomas William Laver, Matthew Neil Wakeling, … Sarah Elizabeth Flanagan·Clinical EndocrinologyPeer-reviewed·Aug 23, 2018