Basic Information
Gene ID
evm.TU.Chr9.2019
Position
GWHBISF00000491:45551008-45568761 (+)
17753bp
Gene Type
gene
Gene Description (Protein Product)
histone-lysine N-methyltransferase; H3 lysine-9 specific
Organism
Also AS AT1G73100

Gene Structure

upstream:

Domain
Database EntryID E-Value Start end InterPro ID Description

Regulation&Interaction
Protein-protein interaction (PPI)
evm.TU.F000124F.61 histone-lysine N-methyltransferase; H3 lysine-9 specific
evm.TU.Chr9.666 Ribose-5-phosphate isomerase
evm.TU.Chr9.666 Belongs to the class-I aminoacyl-tRNA synthetase family
Regulatory gene
evm.TU.Chr1.1507 Developmental protein SEPALLATA 1-like isoform X1
evm.TU.Chr1.508 MADS-box protein
evm.TU.Chr10.1970_evm.TU.Chr10.1971 Floral homeotic 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.
map01100 Metabolic pathways -
map01100 Metabolic pathways -
map00310 Lysine degradation -
map00310 Lysine degradation -
map00260 Glycine, serine and threonine metabolism Serine is derived from 3-phospho-D-glycerate, an intermediate of glycolysis [MD:M00020], and glycine is derived from serine. Threonine is an essential amino acid, which animals cannot synthesize. In bacteria and plants, threonine is derived from aspartate [MD:M00018].