Gene

Ube2w

Species
Rattus norvegicus
Symbol
Ube2w
Name
ubiquitin-conjugating enzyme E2W
Synonyms
  • E2 ubiquitin-conjugating enzyme W
  • LOC100909445
Biotype
protein coding gene
Automated Description
Predicted to enable ubiquitin conjugating enzyme activity and ubiquitin protein ligase binding activity. Predicted to be involved in several processes, including antiviral innate immune response; protein ubiquitination; and proteolysis involved in protein catabolic process. Predicted to be active in nucleus. Orthologous to human UBE2W (ubiquitin conjugating enzyme E2 W).
RGD Description
Predicted to enable ubiquitin conjugating enzyme activity and ubiquitin protein ligase binding activity. Predicted to be involved in several processes, including antiviral innate immune response; protein ubiquitination; and proteolysis involved in protein catabolic process. Predicted to be located in nucleus. Orthologous to human UBE2W (ubiquitin conjugating enzyme E2 W); INTERACTS WITH 1,2-dichloroethane (ortholog); 1,2-dimethylhydrazine (ortholog); 2,2',4,4',5,5'-hexachlorobiphenyl (ortholog).
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR24067
Links to orthology data in JBrowse by filter level: Stringent,  Moderate,  No filter,  Best and Best Reverse

Paralogy

Function - GO Annotations

Pathways

No data available

Phenotypes

Primary Sources
None
Other Sources
None

Disease Associations

Cases where the expected disease association was NOT found
Must provide at least one subject
Cell color indicative of annotation volume

Alleles and Variants

Genome location
Assembly version
mRatBN7.2
Viewer Help
2.70M2.72M2.74M2.76M2.78M2.80M
Variant Types and ConsequencesOnly variants associated to alleles are shown in the graphics above. See all variants in JBrowse.
Allele/Variant Symbol
Allele Synonyms
Category
Variant
Variant type
Molecular consequence
Has Disease Annotations
Has Phenotype Annotations
NC_051340.1:g.2694382A>Cvariant
SNP
  • intron variant
NC_051340.1:g.2704829T>Cvariant
SNP
  • intron variant
NC_051340.1:g.2692757T>Cvariant
SNP
  • intron variant
NC_051340.1:g.2693797A>Gvariant
SNP
  • intron variant
NC_051340.1:g.2709218A>Cvariant
SNP
  • intron variant
NC_051340.1:g.2719205T>Cvariant
SNP
  • intron variant
NC_051340.1:g.2741241A>Gvariant
SNP
  • intron variant
NC_051340.1:g.2776540C>Avariant
SNP
  • intron variant
NC_051340.1:g.2788054T>Avariant
SNP
  • intron variant
NC_051340.1:g.2810359T>Gvariant
SNP
  • intron variant
Showing 1 - 10 of 332 rows
per page

Transgenic Alleles

Models

No data available

Sequence Feature Viewer

Genome location
Assembly version
mRatBN7.2
Viewer Help
2.70M2.72M2.74M2.76M2.78M2.80M

Sequence Details

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Expression

Primary Sources
None
Other Sources
Must provide at least one subject
Cell color indicative of annotation volume; red slash indicates species lacks structure or developmental stage.

Molecular Interactions

Genetic Interactions