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PXD029983

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.
HostingRepositoryPRIDE
AnnounceDate2022-05-04
AnnouncementXMLSubmission_2022-05-04_04:10:29.989.xml
DigitalObjectIdentifier
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
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Dataset FTP location
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PRIDE project URI
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