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PXD029983 is an original dataset announced via ProteomeXchange.

Dataset Summary
TitleDe novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway
DescriptionMain 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.
ReviewLevelPeer-reviewed dataset
DatasetOriginOriginal dataset
RepositorySupportUnsupported dataset by repository
PrimarySubmitterPrerana Wagle
SpeciesList scientific name: Homo sapiens (Human); NCBI TaxID: 9606;
ModificationListphosphorylated residue
InstrumentQ Exactive
Dataset History
RevisionDatetimeStatusChangeLog Entry
02021-11-26 08:40:14ID requested
12022-05-04 04:10:30announced
Publication List
Dataset with its publication pending
Keyword List
submitter keyword: CSNK2B, CK2β and CK2
Contact List
Muhammad Sajid Hussain
contact affiliationCologne Center for Genomics (CCG), University of Cologne, Faculty of Medicine and University Hospital Cologne
contact emailmhussain@uni-koeln.de
lab head
Prerana Wagle
contact affiliationCECAD Research Center
contact emailproteomics-facility@uni-koeln.de
dataset submitter
Full Dataset Link List
Dataset FTP location
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PRIDE project URI
Repository Record List
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