PXD043691 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | Clinical and molecular delineation of classical-like Ehlers–Danlos syndrome through a comprehensive next-generation sequencing-based screening system |
Description | Classical-like Ehlers–Danlos syndrome (clEDS) is an autosomal recessive disorder caused by complete absence of tenascin-X resulting from biallelic variation in TNXB. Accurate detection of TNXB variants is challenging because of the presence of the pseudogene TNXA, which can undergo non-allelic homologous recombination. Therefore, we designed a genetic screening system that is performed using similar operations to other next-generation sequencing (NGS) panel analyses and can be applied to accurately detect TNXB variants and the recombination of TNXA-derived sequences into TNXB. We also analyzed the levels of serum form of TNX (sTNX) by Western bot and LC/MS/MS. Using this system, we identified biallelic TNXB variants in nine unrelated clEDS patients. This report is the first to apply an NGS-based screening for TNXB variants and represents the third largest cohort of clEDS. |
HostingRepository | PRIDE |
AnnounceDate | 2023-08-09 |
AnnouncementXML | Submission_2023-08-08_18:00:50.761.xml |
DigitalObjectIdentifier | |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Unsupported dataset by repository |
PrimarySubmitter | KazuoYamada |
SpeciesList | scientific name: Homo sapiens (Human); NCBI TaxID: 9606; |
ModificationList | No PTMs are included in the dataset |
Instrument | TSQ Quantum Access |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2023-07-11 19:16:41 | ID requested | |
⏵ 1 | 2023-08-08 18:00:51 | announced | |
Publication List
Dataset with its publication pending |
Keyword List
submitter keyword: NGS, LC/MS/MS, Tenascin-X,Classical-like Ehlers–Danlos syndrome |
Contact List
TomomiYamaguchi |
contact affiliation | Shinshu University |
contact email | t_yamaguchi@shinshu-u.ac.jp |
lab head | |
KazuoYamada |
contact affiliation | Department of Legal Medicine, Shimane University |
contact email | yamadak@med.shimane-u.ac.jp |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
NOTE: Most web browsers have now discontinued native support for FTP access within the browser window. But you can usually install another FTP app (we recommend FileZilla) and configure your browser to launch the external application when you click on this FTP link. Or otherwise, launch an app that supports FTP (like FileZilla) and use this address: ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2023/08/PXD043691 |
PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD043691
- Label: PRIDE project
- Name: Clinical and molecular delineation of classical-like Ehlers–Danlos syndrome through a comprehensive next-generation sequencing-based screening system