Accession PRJCA011031
Title Genetic Screen of Congenital Renal Diseases
Relevance Medical
Data types Whole genome sequencing
Organisms Homo sapiens
Description Chronic kidney disease (CKD) is one of the most common renal diseases that present with kidney damage (proteinuria, hematuria, or anatomical abnormality) or a decline in glomerular filtration rate (< 60 mL/min/1.73 m2 for at least 3 months). The CKD incidence rate has recently increased up to 10.8% in China and 14.8% in the United States. As the initial kidney damage progresses to kidney failure, the affected individuals are at an elevated risk of cardiovascular disease and sudden death. Therefore, CKD has become a global public health concern. CKD can be caused by congenital anomalies in the kidneys and urinary tract, steroid-resistant nephrotic syndrome, chronic glomerulonephritis, renal cystic ciliopathies, and urinary stone disease.
Sample scope Multiisolate
Release date 2022-08-05
Publication
PubMed ID Article title Journal name DOI Year
34558151
32903920
35596061
34660292
Grants
Agency program Grant ID Grant title
China Postdoctoral Science Foundation 2020TQ0363
Submitter Hao    Huang  (xyskhuanghao@csu.edu.cn)
Organization Central South University
Submission date 2022-08-05

Project Data

Resource name Description
BioSample (1) -
SAMC2271815 Novel heterozygous mutation in COL4A4 responsible for Alport syndrome in a Chinese family