Species: Hu, Mu
Applications: WB, IHC, IP, ELISA
Host: Mouse Monoclonal
Species: Hu, Mu
Applications: WB, ELISA, ICC/IF, IHC
Host: Rabbit Polyclonal
Species: Hu
Applications: ICC/IF
Host: Rabbit Polyclonal
Species: Hu
Applications: AC
Species: Hu
Applications: AC
Description
Euchromatic histone-lysine N-methyltransferase 1 (EHMT1) is a histone methyltransferase that catalyzes the methylation of lysine-9 of histone H3 (H3-K9). H3-K9 histone methylation is restricted to euchromatin and functions to epigenetically silence gene transcription. Loss of function mutations in EHMT1 cause the 9q34 subtelomeric deletion syndrome, a syndrome characterized by severe mental retardation, hypotonia, brachy(micro)cephaly, heart defects, and distinct facial anomalies. Alternate names for EHMT1 include histone H3-K9 methyltransferase 5, H3-K9-HMTase5, eu-HMTase, G9a-like protein 1, GLP1, lysine N-methyltransferase 1D, EUHMTASE1, KMT1D, and KIAA1876.
Bioinformatics
| Entrez |
Human
|
| Uniprot |
Human
Human
Human
Human
|
| Product By Gene ID |
79813 |
| Alternate Names |
- EC 2.1.1.-
- EC 2.1.1.43
- euchromatic histone-lysine N-methyltransferase 1H3-K9-HMTase 5
- Eu-HMTase1DEL9q34
- EUHMTASE1FP13812
- FLJ12879
- G9a-like protein 1
- GLP
- GLP1
- H3 lysine-9 specific 5
- KIAA1876euchromatic histone methyltransferase 1
- KMT1DDKFZp667M072
|
Research Areas for GLP/EHMT1
Find related products by research area and learn more about each of the different research areas below.
Breast Cancer
