Gene Report
Basic Info
| Approved Symbol |
PPP2R2C
|
| Symbol Alias |
PR52, IMYPNO, MGC33570, PR55G |
| Approved Name |
protein phosphatase 2, regulatory subunit B, gamma |
| Previous Name |
protein phosphatase 2 (formerly 2A), regulatory subunit B (PR 52), gamma isoform, "protein phosphatase 2 (formerly 2A), regulatory subunit B, gamma isoform" |
| Name Alias |
PP2A subunit B isoform gamma |
| Location |
4p16.1 |
| Position |
chr4:6322305-6565327, - |
| External Links |
HGNC: 9306
Entrez Gene: 5522
Ensembl: ENSG00000074211
UCSC: uc003gja.2
|
| No. of Studies |
1 (significant: 1; non-significant: 0; trend: 0) |
| Source |
Literature-origin; Mapped by LD-proxy; Mapped by literature SNP |
Gene related studies (count: 1)
Gene related SNPs (count: 37)
Gene related CNVs (count: 0)
Gene related other variant (count: 0)
Gene related regions (count: 0)
Gene related GO terms (count: 3)
Gene related KEGG pathways (count: 4)
| ID |
Name |
No. of Genes in ADHDgene |
Brief Description |
| hsa05160 |
Hepatitis C |
17 |
Hepatitis C virus (HCV) is a major cause of chronic liver di......
Hepatitis C virus (HCV) is a major cause of chronic liver disease. The HCV employ several strategies to perturb host cell immunity. After invasion, HCV RNA genome functions directly as an mRNA in the cytoplasm of the host cell and forms membrane-associated replication complexes along with non-structural proteins. Viral RNA can trigger the RIG-I pathway and interferon production during this process. Translated HCV protein products regulate immune response to inhibit the action of interferon. HCV core and NS5A proteins appear to be the most important molecules with regulatory functions that modulate transcription, cellular proliferation, and apoptosis.
More...
|
| hsa04530 |
Tight junction |
18 |
Epithelial tight junctions (TJs) are composed of at least th......
Epithelial tight junctions (TJs) are composed of at least three types of transmembrane protein -occludin, claudin and junctional adhesion molecules (JAMs)- and a cytoplasmic 'plaque' consisting of many different proteins that form large complexes. The transmembrane proteins mediate cell adhesion and are thought to constitute the intramembrane and paracellular diffusion barriers. The cytoplasmic 'plaque' contains three major multi-protein complexes consisting largely of scaffolding proteins, the ZO protein complex, the CRB3-Pals1-PATJ complex and the PAR-3-aPKC-PAR-6 complex. The ZO protein complex appears to organize the transmembrane proteins and couple them to other cytoplasmic proteins and to actin microfilaments. Two evolutionarily conserved protein complexes, the CRB3 and PAR complexes are involved in the establishment and maintenance of epithelial cell polarity. Besides these three protein complexes which seem to be constitutively associated at TJs, a number of proteins with different functions has been identified at TJs. These include additional scaffolding proteins like MUPP1 and MAGI-1, adaptor proteins, transcription regulators and RNA processing factors, regulatory proteins like small GTPases and G-proteins, kinases and phosphatases, and heat shock proteins. These are proposed to be involved in junction assembly, barrier regulation, gene transcription, and perhaps other, presently undefined pathways.
More...
|
| hsa03015 |
mRNA surveillance pathway |
17 |
The mRNA surveillance pathway is a quality control mechanism......
The mRNA surveillance pathway is a quality control mechanism that detects and degrades abnormal mRNAs. These pathways include nonsense-mediated mRNA decay (NMD), nonstop mRNA decay (NSD), and no-go decay (NGD). NMD is a mechanism that eliminates mRNAs containing premature translation-termination codons (PTCs). In vertebrates, PTCs trigger efficient NMD when located upstream of an exon junction complex (EJC). Upf3, together with Upf1 and Upf2, may signal the presence of the PTC to the 5'end of the transcript, resulting in decapping and rapid exonucleolytic digestion of the mRNA. In the NSD pathway, which targets mRNAs lacking termination codons, the ribosome is believed to translate through the 3' untranslated region and stall at the end of the poly(A) tail. NSD involves an eRF3-like protein, Ski7p, which is hypothesized to bind the empty A site of the ribosome and recruit the exosome to degrade the mRNA from the 3' end. NGD targets mRNAs with stalls in translation elongation for endonucleolytic cleavage in a process involving the Dom34 and Hbs1 proteins.
More...
|
| hsa05142 |
Chagas disease (American trypanosomiasis) |
23 |
Trypanosoma cruzi is an intracellular protozoan parasite tha......
Trypanosoma cruzi is an intracellular protozoan parasite that causes Chagas disease. The parasite life cycle involves hematophagous reduviid bugs as vectors. Once parasites enter the host body, they invade diverse host cells including cardiomyocytes. Establishment of infection depends on various parasite molecules such as cruzipain, oligopeptidase B, and trans-sialidase that activate Ca2+ signaling. Internalized parasites escape from the parasitophorous vacuole using secreted pore-forming TcTOX molecule and replicate in the cytosol. Multiplied parasites eventually lyse infected host cells and are released in the circulation. During these events, the parasites manipulate host innate immunity and elicit cardiomyocyte hypertrophy. T lymphocyte responses are also disturbed.
More...
|
Genes shared at least 5 GO terms with PPP2R2C (count: 0)
Genes shared at least 2 KEGG pathways with PPP2R2C (count: 9)
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