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Due to system maintenance, the application system, application review by the Data Access Committee will be unavailable during the following period.
Schedule: October 5th (Mon), 2026, 9:00 - October 7th (Wed), 2026, 15:00 (JST)
We apologize for any inconvenience this may cause and appreciate your understanding.

We are currently receiving a large number of applications for data submission, and the review process is taking longer than usual.We sincerely apologize for the delay and kindly ask for your understanding. When submitting an application, we would greatly appreciate it if you could allow sufficient time for the processing.

Following a change to our organizational structure effective April 1, 2026, this division has been renamed from the "Database Center for Life Science, Joint Support-Center for Data Science Research" to the "Database Division for Life Science (DBCLS), BioData Science Initiative (BSI), National Institute of Genetics (NIG)". Where the former name still appears in the guidelines, please read it as the new name.

Research ID

hum0126-v2Release info

Latest

Research title

Identification of the disease and drug susceptibility genes for the Childhood Idiopathic Nephrotic Syndrome

Research overview

Aims
To identify the novel disease susceptibility genes for Childhood Idiopathic Nephrotic Syndrome
Methods
GWAS
Participants/materials
Healthy controls and Childhood Idiopathic Nephrotic Syndrome patients
URL
N/A

Datasets

CartDataset IDType of dataAnalysis methodAccess criteriaDate published
NHA000069GWAS for 224 Childhood Idiopathic Nephrotic Syndrome patients and 419 healthy adult controls
  • Genotyping by array
Unrestricted-access2018-04-27
NHA000153GWAS for 3,206 Childhood Idiopathic Nephrotic Syndrome patients and 987 healthy adult controls
  • Genotyping by array
Unrestricted-access2020-09-01

Data provider

Principal investigator
Kazumoto Iijima
Affiliation
Department of Pediatrics, Kobe University Graduate School of Medicine

Research projects

NameURL
The Research Consortium on Genetics of Childhood Idiopathic Nephrotic Syndrome in Japan
N/A

Grants

NameTitleProject number
Platform Program for Promotion of Genome Medicine, Japan Agency for Medical Research and Development (AMED)
Identification of disease susceptible genes and drug sensitive genes in childhood nephrotic syndrome
  • JP17km0405108
KAKENHI Fund for the Promotion of Joint International Research (Fostering Joint International Research (B))
Joint International Research for identification of disease-susceptible genes and drug-sensitive genes in childhood nephrotic syndrome
  • 18KK0244

Related publications

TitleDOIDataset ID
Strong Association of the HLA-DR/DQ Locus with Childhood Steroid-Sensitive Nephrotic Syndrome in the Japanese Population.
https://doi.org/10.1681/ASN.2017080859 (opens in a new tab)
Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome.
https://doi.org/10.1016/j.kint.2020.05.029 (opens in a new tab)