| Literature DB >> 27157321 |
Brendan Blumenstiel1, Matthew DeFelice2, Ozge Birsoy3, Anthony J Bleyer4, Stanislav Kmoch5, Todd A Carter2, Andreas Gnirke2, Kendrah Kidd4, Heidi L Rehm3, Lucienne Ronco2, Eric S Lander2, Stacey Gabriel2, Niall J Lennon2.
Abstract
Mucin-1 kidney disease, previously described as medullary cystic kidney disease type 1 (MCKD1, OMIM 174000), is an autosomal dominant tubulointerstitial kidney disease recently shown to be caused by a single-base insertion within the variable number tandem repeat region of the MUC1 gene. Because of variable age of disease onset and often subtle signs and symptoms, clinical diagnosis of mucin-1 kidney disease and differentiation from other forms of hereditary kidney disease have been difficult. The causal insertion resides in a variable number tandem repeat region with high GC content, which has made detection by standard next-generation sequencing impossible to date. The inherently difficult nature of this mutation required an alternative method for routine detection and clinical diagnosis of the disease. We therefore developed and validated a mass spectrometry-based probe extension assay with a series of internal controls to detect the insertion event using 24 previously characterized positive samples from patients with mucin-1 kidney disease and 24 control samples known to be wild type for the variant. Validation results indicate an accurate and reliable test for clinically establishing the molecular diagnosis of mucin-1 kidney disease with 100% sensitivity and specificity across 275 tests called.Entities:
Mesh:
Substances:
Year: 2016 PMID: 27157321 DOI: 10.1016/j.jmoldx.2016.03.003
Source DB: PubMed Journal: J Mol Diagn ISSN: 1525-1578 Impact factor: 5.568