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NBDC Human Database

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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

hum0269-v2Release info

Latest

Research title

Sensitive gene analysis of hereditary cardiovascular disease

Research overview

Aims
Elucidation of the pathophysiology of patients with hereditary cardiovascular disease
Methods
Whole exome sequencing analysis and RNA-seq analysis
Participants/materials
hereditary cardiovascular disease

Datasets

CartDataset IDType of dataAnalysis methodAccess criteriaDate published
JGAD000402NGS (Exome, RNA-seq)
  • WES
  • RNA-seq
Controlled-access (Type I)2021-05-24
JGAD000691NGS (Exome)
  • WES
Controlled-access (Type I)2024-03-19
JGAD000692NGS (Exome)
  • WES
Controlled-access (Type I)2024-03-19
JGAD000693NGS (Exome)
  • WES
Controlled-access (Type I)2024-03-19

Data provider

Principal investigator
Yoshihiro Asano
Affiliation
Department of Cardiovascular Medicine, Graduate School of Medicine, Osaka University

Research projects

NameURL
Molecular Genetics and Drug Discovery Group

Grants

NameTitleProject number
KAKENHI Grant-in-Aid for Scientific Research (B)
Identification of de novo molecular targets and drug discovery by genome analysis and trans-omics analysis of hereditary cardiomyopathy
  • 19H03652
KAKENHI Grant-in-Aid for Scientific Research (B)
Functional and informatics integration analysis based on whole genome analysis platform and identification of novel cardiomyopathy genes and elucidation of their mechanisms
  • 22H03067
Research Center Network for Realization of Regenerative Medicine, Japan Agency for Medical Research and Development (AMED)
Development of Autologous Skeletal Myoblast Cell Sheet Transplantation for Dilated Cardiomyopathy Aiming Precision Medicine
  • JP22bm040070
Research Center Network for Realization of Regenerative Medicine, Japan Agency for Medical Research and Development (AMED)
Drug discovery via development of multidisciplinary drug screening system by using disease specific-iPS cells derived from refractory cardiomyopathy
  • JP22bm0804008

Related publications

TitleDOIDataset ID
Loss-of-function mutations in the co-chaperone protein BAG5 cause dilated cardiomyopathy requiring heart transplantation

Controlled access users

Principal investigatorAffiliationCountry/RegionResearch titlePeriod of data useDataset ID
Michiaki HamadaHamada Laboratory, Faculty of Science and Engineering, Waseda UniversityJapanConstruction of RNA-targeted Drug Discovery Database2023-01-05 – 2027-10-31