Identity
HGNC
LOCATION
17q22
LOCUSID
ALIAS
AHUS7,DAGK5,DAGK6,DGK,NPHS7
FUSION GENES
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: 8526
MIM: 601440
HGNC: 2852
Ensembl: ENSG00000153933
Variants:
dbSNP: 8526
ClinVar: 8526
TCGA: ENSG00000153933
COSMIC: DGKE
RNA/Proteins
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38008259 | 2024 | Diacylglycerol kinase-ε is S-palmitoylated on cysteine in the cytoplasmic end of its N-terminal transmembrane fragment. | 0 |
| 38008259 | 2024 | Diacylglycerol kinase-ε is S-palmitoylated on cysteine in the cytoplasmic end of its N-terminal transmembrane fragment. | 0 |
| 36113832 | 2022 | An intact zinc finger motif of the C1B domain is critical for stability and activity of diacylglycerol kinase-ε. | 1 |
| 36113832 | 2022 | An intact zinc finger motif of the C1B domain is critical for stability and activity of diacylglycerol kinase-ε. | 1 |
| 33986189 | 2021 | Loss of diacylglycerol kinase ε causes thrombotic microangiopathy by impairing endothelial VEGFA signaling. | 5 |
| 33986189 | 2021 | Loss of diacylglycerol kinase ε causes thrombotic microangiopathy by impairing endothelial VEGFA signaling. | 5 |
| 32413569 | 2020 | Various phenotypes of disease associated with mutated DGKE gene. | 2 |
| 32413569 | 2020 | Various phenotypes of disease associated with mutated DGKE gene. | 2 |
| 28526779 | 2017 | The Phenotypic Spectrum of Nephropathies Associated with Mutations in Diacylglycerol Kinase ε. | 16 |
| 28526779 | 2017 | The Phenotypic Spectrum of Nephropathies Associated with Mutations in Diacylglycerol Kinase ε. | 16 |
| 25498910 | 2015 | Loss of DGKε induces endothelial cell activation and death independently of complement activation. | 31 |
| 25854283 | 2015 | Characterization of a New DGKE Intronic Mutation in Genetically Unsolved Cases of Familial Atypical Hemolytic Uremic Syndrome. | 26 |
| 26018111 | 2015 | Atypical haemolytic uraemic syndrome in a Japanese patient with DGKE genetic mutations. | 8 |
| 25498910 | 2015 | Loss of DGKε induces endothelial cell activation and death independently of complement activation. | 31 |
| 25854283 | 2015 | Characterization of a New DGKE Intronic Mutation in Genetically Unsolved Cases of Familial Atypical Hemolytic Uremic Syndrome. | 26 |
Citation
Dessen P
DGKE (diacylglycerol kinase epsilon)
Atlas Genet Cytogenet Oncol Haematol. 2007-04-01
Online version: http://atlasgeneticsoncology.org/gene/46638/dgke-(diacylglycerol-kinase-epsilon)
