Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 25895
MIM: 615258
HGNC: 24936
Ensembl: ENSG00000123427
Variants:
dbSNP: 25895
ClinVar: 25895
TCGA: ENSG00000123427
COSMIC: EEF1AKMT3
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000123427 | ENST00000300209 | Q96AZ1 |
| ENSG00000123427 | ENST00000333012 | Q96AZ1 |
| ENSG00000123427 | ENST00000548256 | F8VZI8 |
| ENSG00000123427 | ENST00000551420 | F8W226 |
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 34446611 | 2021 | METTL21B is a prognostic biomarker and potential therapeutic target in low-grade gliomas. | 5 |
| 34446611 | 2021 | METTL21B is a prognostic biomarker and potential therapeutic target in low-grade gliomas. | 5 |
| 28108655 | 2017 | The novel lysine specific methyltransferase METTL21B affects mRNA translation through inducible and dynamic methylation of Lys-165 in human eukaryotic elongation factor 1 alpha (eEF1A). | 52 |
| 28663172 | 2017 | METTL21B Is a Novel Human Lysine Methyltransferase of Translation Elongation Factor 1A: Discovery by CRISPR/Cas9 Knockout. | 24 |
| 28108655 | 2017 | The novel lysine specific methyltransferase METTL21B affects mRNA translation through inducible and dynamic methylation of Lys-165 in human eukaryotic elongation factor 1 alpha (eEF1A). | 52 |
| 28663172 | 2017 | METTL21B Is a Novel Human Lysine Methyltransferase of Translation Elongation Factor 1A: Discovery by CRISPR/Cas9 Knockout. | 24 |
| 22948820 | 2012 | Lysine methylation of VCP by a member of a novel human protein methyltransferase family. | 75 |
| 22948820 | 2012 | Lysine methylation of VCP by a member of a novel human protein methyltransferase family. | 75 |
| 20190274 | 2010 | The multiple sclerosis whole blood mRNA transcriptome and genetic associations indicate dysregulation of specific T cell pathways in pathogenesis. | 62 |
| 20190274 | 2010 | The multiple sclerosis whole blood mRNA transcriptome and genetic associations indicate dysregulation of specific T cell pathways in pathogenesis. | 62 |
Citation
Dessen P
EEF1AKMT3 (EEF1A lysine methyltransferase 3)
Atlas Genet Cytogenet Oncol Haematol. 2017-09-01
Online version: http://atlasgeneticsoncology.org/gene/79777/eef1akmt3-(eef1a-lysine-methyltransferase-3)
