Novel MUC1 variant identified by massively parallel sequencing explains interstitial kidney disease in a large Dutch family
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F23%3A10465391" target="_blank" >RIV/00216208:11110/23:10465391 - isvavai.cz</a>
Result on the web
<a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=pyVlNFuluO" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=pyVlNFuluO</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.kint.2023.02.021" target="_blank" >10.1016/j.kint.2023.02.021</a>
Alternative languages
Result language
angličtina
Original language name
Novel MUC1 variant identified by massively parallel sequencing explains interstitial kidney disease in a large Dutch family
Original language description
Chronic kidney disease (CKD) can be caused by various systemic and kidney disorders with overlapping or nonspecific clinical presentations. Despite a thorough diagnostic workup, the primary cause of CKD remains uncertain in 20% to 35% of affected individuals. Recent studies have demonstrated that massively parallel sequencing (MPS) can be a useful additional tool in the diagnostic workup of patients with unexplained CKD, providing a molecular diagnosis in 11% to 56% of cases. Establishing the correct diagnosis through MPS may not only have therapeutic consequences but may also improve detection of extrarenal manifestations (reverse phenotyping), improve genetic counseling of patients and their relatives, and influence donor selection for (living-related) transplantation. Here, we describe a large Dutch family with interstitial kidney disease of unknown origin in whom we identified a novel frameshift mutation in the MUC1 gene, encoding mucin 1, using an MPS-based multigene panel.
Czech name
—
Czech description
—
Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
—
OECD FORD branch
30101 - Human genetics
Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2023
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Kidney International
ISSN
0085-2538
e-ISSN
1523-1755
Volume of the periodical
103
Issue of the periodical within the volume
5
Country of publishing house
US - UNITED STATES
Number of pages
4
Pages from-to
986-989
UT code for WoS article
000985430900001
EID of the result in the Scopus database
2-s2.0-85152114710