PXD029983 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway |
Description | Main purpose of the project is to delineate the consequences of de novo variants identified in patients manifesting intellectual disability-craniodigital syndrome. To this end, we investigated the effects of mutated CK2β by performing phosphor proteome profiling of patient derived LCLs along with the age and gender matched control. |
HostingRepository | PRIDE |
AnnounceDate | 2022-05-04 |
AnnouncementXML | Submission_2022-05-04_04:10:29.989.xml |
DigitalObjectIdentifier | |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Unsupported dataset by repository |
PrimarySubmitter | Prerana Wagle |
SpeciesList | scientific name: Homo sapiens (Human); NCBI TaxID: 9606; |
ModificationList | phosphorylated residue |
Instrument | Q Exactive |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2021-11-26 08:40:14 | ID requested | |
⏵ 1 | 2022-05-04 04:10:30 | announced | |
Publication List
Dataset with its publication pending |
Keyword List
submitter keyword: CSNK2B, CK2β and CK2 |
Contact List
Muhammad Sajid Hussain |
contact affiliation | Cologne Center for Genomics (CCG), University of Cologne, Faculty of Medicine and University Hospital Cologne |
contact email | mhussain@uni-koeln.de |
lab head | |
Prerana Wagle |
contact affiliation | CECAD Research Center |
contact email | proteomics-facility@uni-koeln.de |
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/2022/05/PXD029983 |
PRIDE project URI |
Repository Record List
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[ - ]
- PRIDE
- PXD029983
- Label: PRIDE project
- Name: De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway