Basic Information
Gene ID
Position
Chr5:180853834-180857799 (+)
3965bp
Gene Type
gene
Gene Description (Protein Product)
Belongs to the mitochondrial carrier (TC 2.A.29) family
Organism
Also AS AT3G05290

Gene Structure

upstream:

Domain
Database EntryID E-Value Start end InterPro ID Description

Regulation&Interaction
Protein-protein interaction (PPI)
CSS0044225.g Belongs to the mitochondrial carrier (TC 2.A.29) family
CSS0021878.g Peroxisome biogenesis protein
CSS0023679.g Peroxisome biogenesis protein 16-like
Regulatory gene
CSS0000128.g tesmin tso1-like cxc
CSS0000233.g ABSCISIC ACID-INSENSITIVE 5-like protein
CSS0000305.g Zinc finger 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
map04146 Peroxisome Peroxisomes are essential organelles that play a key role in redox signalling and lipid homeostasis. They contribute to many crucial metabolic processes such as fatty acid oxidation, biosynthesis of ether lipids and free radical detoxification. The biogenesis of peroxisomes starts with the early peroxins PEX3, PEX16 and PEX19 and proceeds via several steps. The import of membrane proteins into peroxisomes needs PEX19 for recognition, targeting and insertion via docking at PEX3. Matrix proteins in the cytosol are recognized by peroxisomal targeting signals (PTS) and transported to the docking complex at the peroxisomal membrane. Peroxisomes' deficiencies lead to severe and often fatal inherited peroxisomal disorders (PD). PDs are usually classified in two groups. The first group is disorders of peroxisome biogenesis which include Zellweger syndrome, and the second group is single peroxisomal enzyme deficiencies.