Gene

Rnf7l

Species
Mus musculus
Symbol
Rnf7l
Name
ring finger protein 7 like
Synonyms
  • EG631906
  • Gm7075
Biotype
protein coding gene
Automated Description
Predicted to enable NEDD8 ligase activity; cullin family protein binding activity; and ubiquitin protein ligase activity. Predicted to be involved in protein neddylation; protein ubiquitination; and ubiquitin-dependent protein catabolic process. Predicted to be located in cytosol and nucleoplasm. Predicted to be part of Cul5-RING ubiquitin ligase complex. Predicted to be active in nucleus. Orthologous to human RNF7 (ring finger protein 7).
MGI Description
Not Available
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR11210
Stringency:
Additional filters to further constrain the results:
Species Gene symbol Count Best Best reverse
Method
Ensembl ComparaHGNCHieranoidInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidXenbaseZFIN
Homo sapiensRNF75 of 10YesNo  
Rattus norvegicusRnf73 of 9YesNo   
Xenopus tropicalisrnf79 of 9YesYes   
Danio reriornf78 of 10YesYes  
Drosophila melanogasterRoc29 of 9YesYes   
Caenorhabditis elegansrbx-29 of 9YesYes   
Links to orthology data in JBrowse by filter level: Stringent,  Moderate,  No filter,  Best and Best Reverse

Paralogy

Gene symbolRank Alignment Length (aa) Similarity %Identity %Method Count
Method
Ensembl ComparaHGNCInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidSGD
Rnf716 of 9 
Rbx122 of 9 
Anapc1122 of 9 

Function - GO Annotations

No function available for that gene

Pathways

No data available

Phenotypes

Primary Sources
None
Other Sources
No data available

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
GRCm39
Viewer Help
63.25715M63.25720M63.25725M63.25730M63.25735M63.25740M63.25745M63.25750M63.25755M
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_000076.7:g.63257407C>Tvariant
SNP
  • missense variant
NC_000076.7:g.63257445C>Tvariant
SNP
  • missense variant
NC_000076.7:g.63257475G>Avariant
SNP
  • missense variant
NC_000076.7:g.63257520A>Gvariant
SNP
  • 5 prime UTR variant
NC_000076.7:g.63257562A>Gvariant
SNP
  • 5 prime UTR variant
NC_000076.7:g.63257311T>Cvariant
SNP
  • missense variant
NC_000076.7:g.63257367G>Avariant
SNP
  • missense variant
NC_000076.7:g.63257230G>Avariant
SNP
  • missense variant
NC_000076.7:g.63257261A>Gvariant
SNP
  • synonymous variant
NC_000076.7:g.63257395A>Gvariant
SNP
  • missense variant
Showing 1 - 10 of 20 rows
per page

Transgenic Alleles

No data available

Models

No data available

Sequence Feature Viewer

Genome location
Assembly version
GRCm39
Viewer Help
63.25715M63.25720M63.25725M63.25730M63.25735M63.25740M63.25745M63.25750M63.25755M

Sequence Details

Loading...

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

No data available

Genetic Interactions

No data available