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

hum0097-v1Release info

Latest

Research title

Cytogenetic analysis of hematopoietic cells in bone marrow failure syndrome

Research overview

Aims
To elucidate the pathogenicity of aplastic anemia with uniparental disomy in 6p
Methods
Exome sequence analysis
Participants/materials
Patients with aplastic anemia with uniparental disomy in 6p
URL
N/A

Datasets

CartDataset IDType of dataAnalysis methodAccess criteriaDate published
JGAD000094NGS (Exome)
  • WES
Controlled-access (Type I)2020-09-28

Data provider

Principal investigator
Shinji Nakao
Affiliation
Cellular Transplantation Biology, Faculty of Medicine, Institute of Medical, Pharmaceutical and Health Sciences, Kanazawa University. Graduate School of Medical Sciences

Research projects

No research projects.

Grants

NameTitleProject number
KAKENHI Grant-in-Aid for Scientific Research (B)
Analysis of clonal hematopoiesis in patients with aplastic anemia
  • 16H05335
KAKENHI Grant-in-Aid for Scientific Research (B)
Identification of hematopoiesis regulator with genomic abnormality in patients with aplastic anemia
  • 24390243

Related publications

TitleDOIDataset ID
Identification of an HLA class I allele closely involved in the autoantigen presentation in acquired aplastic anemia.
https://doi.org/10.1182/blood-2016-11-752378 (opens in a new tab)
N/A
Clinical significance and origin of leukocytes that lack HLA-A allele expression in patients with acquired aplastic anemia.
https://doi.org/10.1016/j.exphem.2016.05.013 (opens in a new tab)
N/A
Somatic Mutations and Clonal Hematopoiesis in Aplastic Anemia.
https://doi.org/10.1056/NEJMoa1414799 (opens in a new tab)
N/A
Frequent loss of HLA alleles associated with copy number-neutral 6pLOH in acquired aplastic anemia.
https://doi.org/10.1182/blood-2011-07-365189 (opens in a new tab)
N/A
Sustained clonal hematopoiesis by HLA-lacking hematopoietic stem cells without driver mutations in aplastic anemia..
https://doi.org/10.1182/bloodadvances.2017013953 (opens in a new tab)

Controlled access users

No use of the controlled access data has been recorded.