Basic Information
Gene ID
JcaChr16G11131.g
Position
chr16:14638334-14640081 (-)
1747bp
Gene Type
gene
Gene Description (Protein Product)
Eukaryotic peptide chain release factor GTP-binding subunit
Organism
Also AS AT1G18070

Gene Structure

upstream:

Domain
Database EntryID E-Value Start end InterPro ID Description

Regulation&Interaction
Protein-protein interaction (PPI)
JcaChr16G11305.g eukaryotic translation initiation factor isoform
JcaChr16G11408.g 116 kDa U5 small nuclear ribonucleoprotein
JcaChr16G11357.g Belongs to the eukaryotic ribosomal protein eS12 family
Regulatory gene
JcaChr01G10034.g Homeobox-leucine zipper protein
JcaChr01G10084.g Homeobox-leucine zipper protein GLABRA
JcaChr01G10422.g (NAC) domain-containing protein

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Annotation

Orthologous Group
Orthologous ID Species Number All hits in PereRegDB Hits of this species Orthologous Detail

Expression Profile
DataSet Number of Samples expressed(TPM>1) Mean Min Max Standard deviation(SD) Coeffcient variation(CV)


Pathway
KEGG Term Name Description
map03015 mRNA surveillance pathway 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.