Mus musculus Gene: Ehmt2
Summary
InnateDB Gene IDBG-174783.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Ehmt2
Gene Name euchromatic histone lysine N-methyltransferase 2
Synonyms Bat8; D17Ertd710e; G9a; KMT1C; NG36
Species Mus musculus
Ensembl Gene ENSMUSG00000013787
Encoded Proteins
euchromatic histone lysine N-methyltransferase 2
euchromatic histone lysine N-methyltransferase 2
euchromatic histone lysine N-methyltransferase 2
euchromatic histone lysine N-methyltransferase 2
euchromatic histone lysine N-methyltransferase 2
euchromatic histone lysine N-methyltransferase 2
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
InnateDB Annotation
Summary
Ehmt2 catalyzes di-methylation of histone H3 at the promoter of interferon (IFN) and IFN-inducible antiviral genes as an epigenetic silencing mechanism in fibroblasts. Ablation of Ehmt2 results in phenotypic conversion to potent IFN-producing cells and renders resistance to RNA viruses.
InnateDB Annotation from Orthologs
Summary
[Homo sapiens] EHMT2 catalyzes di-methylation of histone H3 at the promoter of interferon (IFN) and IFN-inducible antiviral genes as an epigenetic silencing mechanism in fibroblasts. Ablation of EHMT2 results in phenotypic conversion to potent IFN-producing cells and renders resistance to RNA viruses. (Demonstrated in mice)
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000204371:
A cluster of genes, BAT1-BAT5, has been localized in the vicinity of the genes for TNF alpha and TNF beta. This gene is found near this cluster; it was mapped near the gene for C2 within a 120-kb region that included a HSP70 gene pair. These genes are all within the human major histocompatibility complex class III region. This gene was thought to be two different genes, NG36 and G9a, adjacent to each other but a recent publication shows that there is only a single gene. The protein encoded by this gene is thought to be involved in intracellular protein-protein interaction. There are three alternatively spliced transcript variants of this gene but only two are fully described. [provided by RefSeq, Jul 2008]
This gene is located in a gene cluster within the human major histocompatibility complex class III region on chromosome 6. This gene was thought to be two different genes, NG36 and G9a, adjacent to each other but recent publications show that there is only a single gene at this locus. The encoded protein is a histone methyltransferase, which may be involved in repression of transcription. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]
Gene Information
Type Protein coding
Genomic Location Chromosome 17:34898469-34914052
Strand Forward strand
Band B1
Transcripts
ENSMUST00000078061 ENSMUSP00000077208
ENSMUST00000097342 ENSMUSP00000094955
ENSMUST00000013931 ENSMUSP00000013931
ENSMUST00000114033 ENSMUSP00000109667
ENSMUST00000146418
ENSMUST00000138500
ENSMUST00000150786
ENSMUST00000145624
ENSMUST00000124846 ENSMUSP00000121838
ENSMUST00000131915
ENSMUST00000137071 ENSMUSP00000134749
ENSMUST00000145201
ENSMUST00000124002
ENSMUST00000172921 ENSMUSP00000134089
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 27 experimentally validated interaction(s) in this database.
They are also associated with 74 interaction(s) predicted by orthology.
Experimentally validated
Total 28 [view]
Protein-Protein 25 [view]
Protein-DNA 3 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 74 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0002039 p53 binding
GO:0005515 protein binding
GO:0008270 zinc ion binding
GO:0018024 histone-lysine N-methyltransferase activity
GO:0046974 histone methyltransferase activity (H3-K9 specific)
GO:0046976 histone methyltransferase activity (H3-K27 specific)
GO:0070742 C2H2 zinc finger domain binding
Biological Process
GO:0000122 negative regulation of transcription from RNA polymerase II promoter
GO:0006275 regulation of DNA replication
GO:0006306 DNA methylation
GO:0006357 regulation of transcription from RNA polymerase II promoter
GO:0007130 synaptonemal complex assembly
GO:0007281 germ cell development
GO:0007286 spermatid development
GO:0009566 fertilization
GO:0010424 DNA methylation on cytosine within a CG sequence
GO:0016571 histone methylation
GO:0018027 peptidyl-lysine dimethylation
GO:0034968 histone lysine methylation
GO:0035265 organ growth
GO:0045087 innate immune response (InnateDB)
GO:0051567 histone H3-K9 methylation
GO:0070734 histone H3-K27 methylation
Cellular Component
GO:0005634 nucleus
GO:0005694 chromosome
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
REACTOME
RNA Polymerase I Transcription pathway
RNA Polymerase I, RNA Polymerase III, and Mitochondrial Transcription pathway
Cellular responses to stress pathway
Cellular Senescence pathway
Senescence-Associated Secretory Phenotype (SASP) pathway
Gene Expression pathway
RNA Polymerase I Promoter Clearance pathway
RNA Polymerase I Transcription Initiation pathway
KEGG
Lysine degradation pathway
INOH
PID NCI
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
RNA Polymerase I Transcription Initiation pathway
Cellular responses to stress pathway
RNA Polymerase I Transcription pathway
RNA Polymerase I Promoter Clearance pathway
Cellular Senescence pathway
RNA Polymerase I, RNA Polymerase III, and Mitochondrial Transcription pathway
Senescence-Associated Secretory Phenotype (SASP) pathway
Gene Expression pathway
KEGG
Lysine degradation pathway
INOH
PID NCI
Regulation of Androgen receptor activity
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Mm.35345
RefSeq NM_001286573 NM_001286575 NM_145830 NM_147151
OMIM
CCDS CCDS28666 CCDS28667 CCDS70797 CCDS70798
HPRD
IMGT
MGI ID
MGI Symbol
EMBL
GenPept
RNA Seq Atlas