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ProteomicsTBCK, PPP1R21, and C12orf4-interaction AP-MS
To indentify the interaction protein of TBCK, PPP1R21, and C12orf4 by purification of flagg-tagged ones coupled mass spectrum
ORGANISM(S): Homo sapiens (Human) 
2026-03-02 | PXD053078 | Pride
Tbck And c12orf4-interaction ap-ms Ppp1r21 
UnknownExpanding the phenotype of PPP1R21-related neurodevelopmental disorder.
Not available
S-EPMC11065596 | biostudies-literature
UnknownObesity-Dependent Association of the rs10454142 PPP1R21 with Breast Cancer.
Not available
S-EPMC11048332 | biostudies-literature
UnknownBiallelic loss of function variants in PPP1R21 cause a neurodevelopmental syndrome with impaired endocytic function.
Not available
S-EPMC6370506 | biostudies-literature
ProteomicsA homozygous PPP1R21 splice variant associated with severe developmental delay, absence of speech and muscle weakness leads to activated proteasome function
PPP1R21 acts as a co-factor for protein phosphatase 1 (PP1), an important serine/threonine phosphatase known to be essential for cell division, control of glycogen metabolism, protein synthesis and muscle contractility. Bi-allelic pathogenic variants in PPP1R21 were linked to a neurodevelopmental di...
ORGANISM(S): Homo sapiens (Human) 
2023-05-10 | PXD034993 | Pride
Congenital Chkb  choline/ethanolamine kinase  muscular dystrophy Megaconial type (mdcmc)  vapb 
UnknownA Homozygous PPP1R21 Splice Variant Associated with Severe Developmental Delay, Absence of Speech, and Muscle Weakness Leads to Activated Proteasome Function.
Not available
S-EPMC10039818 | biostudies-literature
UnknownRegulatory polymorphisms of <i>MSH6</i>, <i>MSH2</i>, <i>FBXO11,</i> and <i>PPP1R21</i> genes affect survival of patients with immunotherapy-treated lung cancer.
Not available
S-EPMC12406856 | biostudies-literature
UnknownNeurogenetic disorders associated with mutations in the FERRY complex: a novel disease class?
Not available
S-EPMC11928052 | biostudies-literature
UnknownSex-Hormone-Binding Globulin Gene Polymorphisms and Breast Cancer Risk in Caucasian Women of Russia.
Not available
S-EPMC10888713 | biostudies-literature
UnknownTBCK-deficiency leads to compartment-specific mRNA and lysosomal trafficking defects in patient-derived neurons.
Not available
S-EPMC11908138 | biostudies-literature
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