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: 148581
HGNC: 28559
Ensembl: ENSG00000177414
Variants:
dbSNP: 148581
ClinVar: 148581
TCGA: ENSG00000177414
COSMIC: UBE2U
RNA/Proteins
Expression (GTEx)
Pathways
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 33776059 | 2021 | Whole exome sequencing reveals putatively novel associations in retinopathies and drusen formation. | 2 |
| 33776059 | 2021 | Whole exome sequencing reveals putatively novel associations in retinopathies and drusen formation. | 2 |
| 27903633 | 2017 | An E2-guided E3 Screen Identifies the RNF17-UBE2U Pair as Regulator of the Radiosensitivity, Immunodeficiency, Dysmorphic Features, and Learning Difficulties (RIDDLE) Syndrome Protein RNF168. | 4 |
| 27903633 | 2017 | An E2-guided E3 Screen Identifies the RNF17-UBE2U Pair as Regulator of the Radiosensitivity, Immunodeficiency, Dysmorphic Features, and Learning Difficulties (RIDDLE) Syndrome Protein RNF168. | 4 |
Citation
Dessen P
UBE2U (ubiquitin conjugating enzyme E2 U)
Atlas Genet Cytogenet Oncol Haematol. 2015-02-01
Online version: http://atlasgeneticsoncology.org/gene/54994/ube2u-(ubiquitin-conjugating-enzyme-e2-u)
