UBE2V2
Ubiquitin-conjugating enzyme E2 variant 2
Also known as: DDVit-1, DDVIT1, EDAF-1, EDPF-1, EDPF1, MMS2, UB2V2_HUMAN, UEV-2, UEV2
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q15819
- Gene
- UBE2V2
- Ensembl
- ENSG00000169139
- Chromosome
- 8
- Canonical length
- 145 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
Ubiquitin-conjugating enzyme E2 variant proteins constitute a distinct subfamily within the E2 protein family. They have sequence similarity to other ubiquitin-conjugating enzymes but lack the conserved cysteine residue that is critical for the catalytic activity of E2s. The protein encoded by this gene also shares homology with ubiquitin-conjugating enzyme E2 variant 1 and yeast MMS2 gene product. It may be involved in the differentiation of monocytes and enterocytes. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
145 residues, UniProt reviewed canonical sequence.
>Q15819|UBE2V2
1 MAVSTGVKVP RNFRLLEELE EGQKGVGDGT VSWGLEDDED MTLTRWTGMI IGPPRTNYEN
61 RIYSLKVECG PKYPEAPPSV RFVTKINMNG INNSSGMVDA RSIPVLAKWQ NSYSIKVVLQ
121 ELRRLMMSKE NMKLPQPPEG QTYNNLocalizationUniProt · AlphaFold · HPA
Whether an antibody against UBE2V2 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.32
- Highest tissue expression
- 30 nTPM
Expression across tissuesHPA
Tissue
- cerebral cortex: 30 nTPM
- skeletal muscle: 27 nTPM
- liver: 25 nTPM
- tongue: 23 nTPM
- retina: 20 nTPM
- esophagus: 19 nTPM
Single-cell type
- esophageal apical cells: 401 nCPM
- esophageal suprabasal cells: 293 nCPM
- megakaryocytes: 229 nCPM
- syncytiotrophoblasts: 192 nCPM
- extravillous trophoblasts: 186 nCPM
- late primary spermatocytes: 170 nCPM
Immune cell
- NK-cell: 53 nTPM
- T-reg: 45 nTPM
- total PBMC: 41 nTPM
- intermediate monocyte: 41 nTPM
- myeloid DC: 40 nTPM
- naive CD8 T-cell: 38 nTPM
Brain region
- cerebral cortex: 34 nTPM
- thalamus: 33 nTPM
- pons: 32 nTPM
- hypothalamus: 31 nTPM
- midbrain: 31 nTPM
- medulla oblongata: 30 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.25
- gnomAD pLI
- 0.03
- gnomAD missense Z
- 1.33
- DepMap mean gene effect
- -0.14
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 15% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- DNA damage tolerance
- DNA double-strand break processing
- error-free postreplication DNA repair
- positive regulation of double-strand break repair
- positive regulation of protein K63-linked ubiquitination
- protein K63-linked ubiquitination
- protein polyubiquitination
- protein ubiquitination
- regulation of DNA repair
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of UBE2V2 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads UBE2V2 as an antibody target. Whether an autoantibody or antibody against UBE2V2 could matter depends on whether native UBE2V2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
UBE2V2 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label UBE2V2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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