Aliases for PPP4C Gene
External Ids for PPP4C Gene
Previous GeneCards Identifiers for PPP4C Gene
GeneCards Summary for PPP4C Gene
PPP4C (Protein Phosphatase 4 Catalytic Subunit) is a Protein Coding gene. Diseases associated with PPP4C include lipodystrophy, congenital generalized, type 3 and partial lipodystrophy, congenital cataracts, and neurodegeneration syndrome. Among its related pathways are Glucagon signaling pathway and DNA Double-Strand Break Repair. GO annotations related to this gene include hydrolase activity and protein serine/threonine phosphatase activity. An important paralog of this gene is PPP2CB.
UniProtKB/Swiss-Prot for PPP4C Gene
Protein phosphatase that is involved in many processes such as microtubule organization at centrosomes, maturation of spliceosomal snRNPs, apoptosis, DNA repair, tumor necrosis factor (TNF)-alpha signaling, activation of c-Jun N-terminal kinase MAPK8, regulation of histone acetylation, DNA damage checkpoint signaling, NF-kappa-B activation and cell migration. The PPP4C-PPP4R1 PP4 complex may play a role in dephosphorylation and regulation of HDAC3. The PPP4C-PPP4R2-PPP4R3A PP4 complex specifically dephosphorylates H2AFX phosphorylated on Ser-140 (gamma-H2AFX) generated during DNA replication and required for DNA double strand break repair. Dephosphorylates NDEL1 at CDK1 phosphorylation sites and negatively regulates CDK1 activity in interphase (By similarity). In response to DNA damage, catalyzes RPA2 dephosphorylation, an essential step for DNA repair since it allows the efficient RPA2-mediated recruitment of RAD51 to chromatin.