Skip to content
NBDC Human Database

No datasets in the cart.

Go to the cart

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

hum0029-v2Release info

Latest

Research title

Study of Genome Polymorphism/Variation on Stevens-Johnson Syndrome

Research overview

Aims
Identification of new susceptibility gene(s) to cole medicine-related Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN)
Methods
SNP-based and SNV/INDEL/structural variation-based genome-wide association study.
Participants/materials
Patients with cold medicine-related SJS/TEN and healthy controls
URL
N/A

Datasets

CartDataset IDType of dataAnalysis methodAccess criteriaDate published
NHA000049GWAS for SJS
  • Genotyping by array
Unrestricted-access2016-03-09
NHA000155GWAS for SJS/TEN
  • Genotyping by array
Unrestricted-access2020-12-21

Data provider

Principal investigator
Mayumi Ueta
Affiliation
Kyoto Prefectural University of Medicine

Research projects

NameURL
Department of Frontier Medical Science and Technology for Ophthalmology

Grants

NameTitleProject number
KAKENHI Grant-in-Aid for Scientific research (B)
Pioneering research for elucidation of pathogenic mechanism and prediction of onset risk
  • 22390325
KAKENHI Grant-in-Aid for Scientific Research on Innovative Areas
Genome Science
  • 221S0002
Tailor-made Medical Treatment Program (BioBank Japan: BBJ)
Genetic and Pathogenic studies on cold medicine-related severe drug adverse reactions
N/A

Related publications

TitleDOIDataset ID
IKZF1, a new susceptibility gene for cold medicine-related Stevens-Johnson syndrome/toxic epidermal necrolysis with severe mucosal involvement.
https://doi.org/10.1016/j.jaci.2014.12.1916 (opens in a new tab)
Mapping of susceptible variants for cold medicine-related Stevens-Johnson syndrome by whole-genome resequencing
https://doi.org/10.1038/s41525-021-00171-2 (opens in a new tab)