Basic Information
Gene ID
Ciclev10021960m.g.v1.0
Position
scaffold_3:5606601-5609366 (+)
2765bp
Gene Type
gene
Gene Description (Protein Product)
Peroxisome biogenesis protein
Organism
Also AS AT5G17550CICLE_v10021960mg

Gene Structure

upstream:

Domain
Database EntryID E-Value Start end InterPro ID Description

Regulation&Interaction
Protein-protein interaction (PPI)
Ciclev10024720m.g.v1.0 ABC transporter D family member
Ciclev10025877m.g.v1.0 Peroxisome biogenesis factor
Ciclev10024320m.g.v1.0 Peroxisomal membrane protein
Regulatory gene
Ciclev10001400m.g.v1.0 Protein BASIC PENTACYSTEINE6-like
Ciclev10001730m.g.v1.0 transcription factor
Ciclev10002179m.g.v1.0 dof zinc finger protein

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Annotation

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


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.