The protein encoded by this gene is a histone methyltransferase that methylates the lysine-9 position of histone H3. This action marks the genomic region packaged with these methylated histones for transcriptional repression. This protein may be involved in the silencing of MYC- and E2F-responsive genes and therefore could play a role in the G0/G1 cell cycle transition. Defects in this gene are a cause of chromosome 9q subtelomeric deletion syndrome (9q-syndrome, also known as Kleefstra syndrome). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2017]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| EHMT1-20-RE | 20 (40 μL) | 200 μL |  |
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| EHMT1-20-OR | 20 (40 μL) | 200 μL |  |
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| EHMT1-20-GO | 20 (40 μL) | 200 μL |  |
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| EHMT1-20-GR | 20 (40 μL) | 200 μL |  |
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| EHMT1-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene is a histone methyltransferase that methylates the lysine-9 position of histone H3. This action marks the genomic region packaged with these methylated histones for transcriptional repression. This protein may be involved in the silencing of MYC- and E2F-responsive genes and therefore could play a role in the G0/G1 cell cycle transition. Defects in this gene are a cause of chromosome 9q subtelomeric deletion syndrome (9q-syndrome, also known as Kleefstra syndrome). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2017]
Gene Symbol : EHMT1
Gene Name : Euchromatic histone lysine methyltransferase 1
Chromosome : CHR 9: 137,618,987-137,836,126
Locus : 9q34.3
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