Mus musculus Gene: Ppp2r5e
Summary
InnateDB Gene IDBG-149228.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Ppp2r5e
Gene Name protein phosphatase 2, regulatory subunit B (B56), epsilon isoform
Synonyms 4633401M22Rik; AI449017; B56beta
Species Mus musculus
Ensembl Gene ENSMUSG00000021051
Encoded Proteins
protein phosphatase 2, regulatory subunit B (B56), epsilon isoform
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000154001:
The product of this gene belongs to the phosphatase 2A regulatory subunit B family. Protein phosphatase 2A is one of the four major Ser/Thr phosphatases, and it is implicated in the negative control of cell growth and division. It consists of a common heteromeric core enzyme, which is composed of a catalytic subunit and a constant regulatory subunit, that associates with a variety of regulatory subunits. The B regulatory subunit might modulate substrate selectivity and catalytic activity. This gene encodes an epsilon isoform of the regulatory subunit B56 subfamily. [provided by RefSeq, Jul 2008]
The protein encoded by this gene belongs to the phosphatase 2A regulatory subunit B family. Protein phosphatase 2A is one of the four major Ser/Thr phosphatases, and it is implicated in the negative control of cell growth and division. It consists of a common heteromeric core enzyme, which is composed of a catalytic subunit and a constant regulatory subunit, that associates with a variety of regulatory subunits. The B regulatory subunit might modulate substrate selectivity and catalytic activity. This gene encodes an epsilon isoform of the regulatory subunit B56 subfamily. Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Aug 2013]
Gene Information
Type Protein coding
Genomic Location Chromosome 12:75450883-75596200
Strand Reverse strand
Band C3
Transcripts
ENSMUST00000021447 ENSMUSP00000021447
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 2 experimentally validated interaction(s) in this database.
They are also associated with 20 interaction(s) predicted by orthology.
Experimentally validated
Total 2 [view]
Protein-Protein 2 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 20 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005488 binding
GO:0005515 protein binding
GO:0008601 protein phosphatase type 2A regulator activity
Biological Process
GO:0007165 signal transduction
GO:0050790 regulation of catalytic activity
Cellular Component
GO:0000159 protein phosphatase type 2A complex
GO:0005737 cytoplasm
GO:0043231 intracellular membrane-bounded organelle
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
REACTOME
Cell Cycle, Mitotic pathway
Disease pathway
deletions in the AMER1 gene destabilize the destruction complex pathway
Signaling by Wnt pathway
Separation of Sister Chromatids pathway
Resolution of Sister Chromatid Cohesion pathway
Beta-catenin phosphorylation cascade pathway
Signaling by WNT in cancer pathway
Degradation of beta-catenin by the destruction complex pathway
AMER1 mutants destabilize the destruction complex pathway
Cell Cycle pathway
Immune System pathway
M Phase pathway
AXIN mutants destabilize the destruction complex, activating WNT signaling pathway
T41 mutants of beta-catenin aren't phosphorylated pathway
APC truncation mutants have impaired AXIN binding pathway
misspliced LRP5 mutants have enhanced beta-catenin-dependent signaling pathway
RNF mutants show enhanced WNT signaling and proliferation pathway
phosphorylation site mutants of CTNNB1 are not targeted to the proteasome by the destruction complex pathway
disassembly of the destruction complex and recruitment of AXIN to the membrane pathway
deletions in the AXIN genes in hepatocellular carcinoma result in elevated WNT signaling pathway
S37 mutants of beta-catenin aren't phosphorylated pathway
AXIN missense mutants destabilize the destruction complex pathway
TCF dependent signaling in response to WNT pathway
Costimulation by the CD28 family pathway
Mitotic Metaphase and Anaphase pathway
Mitotic Prometaphase pathway
APC truncation mutants are not K63 polyubiquitinated pathway
S45 mutants of beta-catenin aren't phosphorylated pathway
misspliced GSK3beta mutants stabilize beta-catenin pathway
TCF7L2 mutants don't bind CTBP pathway
CTLA4 inhibitory signaling pathway
Adaptive Immune System pathway
truncations of AMER1 destabilize the destruction complex pathway
Signal Transduction pathway
truncated APC mutants destabilize the destruction complex pathway
S33 mutants of beta-catenin aren't phosphorylated pathway
Mitotic Anaphase pathway
XAV939 inhibits tankyrase, stabilizing AXIN pathway
KEGG
Oocyte meiosis pathway
mRNA surveillance pathway pathway
INOH
Insulin receptor signaling pathway
GPCR Dopamine D1like receptor signaling pathway pathway
PID NCI
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
Resolution of Sister Chromatid Cohesion pathway
Mitotic Prometaphase pathway
Separation of Sister Chromatids pathway
CTLA4 inhibitory signaling pathway
Costimulation by the CD28 family pathway
Platelet sensitization by LDL pathway
Platelet homeostasis pathway
Beta-catenin phosphorylation cascade pathway
Degradation of beta-catenin by the destruction complex pathway
truncated APC mutants destabilize the destruction complex pathway
AXIN mutants destabilize the destruction complex, activating WNT signaling pathway
APC truncation mutants are not K63 polyubiquitinated pathway
AMER1 mutants destabilize the destruction complex pathway
misspliced LRP5 mutants have enhanced beta-catenin-dependent signaling pathway
Signaling by WNT in cancer pathway
AXIN missense mutants destabilize the destruction complex pathway
Signaling by Wnt pathway
disassembly of the destruction complex and recruitment of AXIN to the membrane pathway
APC truncation mutants have impaired AXIN binding pathway
T41 mutants of beta-catenin aren't phosphorylated pathway
Signal Transduction pathway
misspliced GSK3beta mutants stabilize beta-catenin pathway
S45 mutants of beta-catenin aren't phosphorylated pathway
deletions in the AMER1 gene destabilize the destruction complex pathway
Cell Cycle pathway
Adaptive Immune System pathway
Immune System pathway
S33 mutants of beta-catenin aren't phosphorylated pathway
truncations of AMER1 destabilize the destruction complex pathway
M Phase pathway
Mitotic Anaphase pathway
phosphorylation site mutants of CTNNB1 are not targeted to the proteasome by the destruction complex pathway
TCF dependent signaling in response to WNT pathway
deletions in the AXIN genes in hepatocellular carcinoma result in elevated WNT signaling pathway
Cell Cycle, Mitotic pathway
RNF mutants show enhanced WNT signaling and proliferation pathway
TCF7L2 mutants don't bind CTBP pathway
XAV939 inhibits tankyrase, stabilizing AXIN pathway
S37 mutants of beta-catenin aren't phosphorylated pathway
Disease pathway
Hemostasis pathway
Mitotic Metaphase and Anaphase pathway
APC truncation mutants have impaired AXIN binding pathway
Signaling by Wnt pathway
Signaling by WNT in cancer pathway
S33 mutants of beta-catenin aren't phosphorylated pathway
M Phase pathway
Costimulation by the CD28 family pathway
Separation of Sister Chromatids pathway
TCF dependent signaling in response to WNT pathway
misspliced LRP5 mutants have enhanced beta-catenin-dependent signaling pathway
S37 mutants of beta-catenin aren't phosphorylated pathway
deletions in the AXIN genes in hepatocellular carcinoma result in elevated WNT signaling pathway
Mitotic Metaphase and Anaphase pathway
Mitotic Anaphase pathway
phosphorylation site mutants of CTNNB1 are not targeted to the proteasome by the destruction complex pathway
Immune System pathway
Cell Cycle, Mitotic pathway
truncations of AMER1 destabilize the destruction complex pathway
AXIN mutants destabilize the destruction complex, activating WNT signaling pathway
XAV939 inhibits tankyrase, stabilizing AXIN pathway
Beta-catenin phosphorylation cascade pathway
CTLA4 inhibitory signaling pathway
Cell Cycle pathway
Signal Transduction pathway
AXIN missense mutants destabilize the destruction complex pathway
misspliced GSK3beta mutants stabilize beta-catenin pathway
disassembly of the destruction complex and recruitment of AXIN to the membrane pathway
TCF7L2 mutants don't bind CTBP pathway
deletions in the AMER1 gene destabilize the destruction complex pathway
AMER1 mutants destabilize the destruction complex pathway
Resolution of Sister Chromatid Cohesion pathway
Adaptive Immune System pathway
RNF mutants show enhanced WNT signaling and proliferation pathway
S45 mutants of beta-catenin aren't phosphorylated pathway
Mitotic Prometaphase pathway
APC truncation mutants are not K63 polyubiquitinated pathway
Disease pathway
Degradation of beta-catenin by the destruction complex pathway
T41 mutants of beta-catenin aren't phosphorylated pathway
truncated APC mutants destabilize the destruction complex pathway
KEGG
Oocyte meiosis pathway
mRNA surveillance pathway pathway
INOH
Insulin receptor signaling pathway
GPCR Dopamine D1like receptor signaling pathway pathway
PID NCI
Cross-References
SwissProt Q61151
TrEMBL
UniProt Splice Variant
Entrez Gene 26932
UniGene Mm.259626
RefSeq NM_012024 XM_006515925 XM_006515926
OMIM
CCDS CCDS25983
HPRD
IMGT
MGI ID MGI:1349473
MGI Symbol Ppp2r5e
EMBL AK088366 AK132432 AK220163 BC085149 U49728
GenPept AAB37234 AAH85149 BAC40306 BAD90335 BAE21166
RNA Seq Atlas 26932