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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

hum0431-v1Release info

Latest

Research title

Genetic analysis aimed at elucidating the pathophysiology, vulnerability to onset, treatment responsiveness of neuropsychiatric disorders, and developing new treatments and diagnostic and preventive methods

Research overview

Aims
Identification of susceptibility gene clusters for neuropsychiatric disorders such as schizophrenia, mood disorders (bipolar disorder, major depressive disorder), developmental disorders, and epilepsy.
Methods
RNA-seq analysis
Participants/materials
We introduced single variants identified in patients with Autism Spectrum Disorder (ASD) into human iPSCs (HPS4290:201B7-Ff]) using the CRISPR/Cas9 system. Variants at the protospacer adjacent motif (PAM) sequence were also introduced.
1) Mutant iPSC lines with the chr7:g.26200781C>T variant and the single PAM sequence: 2 samples
Control lines with a single PAM sequence: 2 samples
2) Mutant iPSC lines with the chr22:g.19179942C>T variant and the single PAM sequence: 3 samples
Control lines with a single PAM sequence: 2 samples
URL
N/A

Datasets

CartDataset IDType of dataAnalysis methodAccess criteriaDate published
JGAD000781NGS (RNA-seq)
  • RNA-seq
Controlled-access (Type I)2024-01-25

Data provider

Principal investigator
Atsushi Takata
Affiliation
Laboratory for Molecular Pathology of Psychiatric Disorders, RIKEN Center for Brain Science

Research projects

No research projects.

Grants

NameTitleProject number
Strategic Research Program for Brain Sciences, Japan Agency for Medical Research and Development (AMED)
Identification of genetically defined subgroups of bipolar disorder by sequence analysis of trio samples
  • JP20dm0107133
Advanced Genome Research and Bioinformatics Study to Facilitate Medical Innovation (GRIFIN), Platform Program for Promotion of Genome Medicine, Japan Agency for Medical Research and Development (AMED)
Analysis of the genetic architectures of human diseases based on the oligogenic model
  • JP22km0405214
The Strategic International Brain Science Research Promotion Program (Brain/MINDS Beyond), Japan Agency for Medical Research and Development (AMED)
Analysis of somatic mutations in bipolar disorder and methodological development of genomic neuropathology
  • JP20dm0307028
KAKENHI Grant-in-Aid for Transformative Research Areas (B)
Identification of genes and key molecular pathways determining cluster/hub cells and analysis of their relationship to human diseases
  • 20H05777
KAKENHI Grant-in-Aid for Scientific Research (B)
Comprehensive study of rare germline and somatic mutations by large-scale sequence analysis for bipolar disorder
  • 21H02855
KAKENHI Grant-in-Aid for Early-Career Scientists
Molecular pathological analysis of a histone methyltransferase associated with autism spectrum disorder
  • 21K15752
KAKENHI Grant-in-Aid for Research Activity Start-up
Identification of loci associated with paternal age effect of Denovo mutation by large-scale family genome data analysis
  • 22K20751

Related publications

TitleDOIDataset ID
Topologically associating domains define the impact of de novo promoter variants on autism spectrum disorder risk

Controlled access users

No use of the controlled access data has been recorded.