Gene

Ubap1

Species
Rattus norvegicus
Symbol
Ubap1
Name
ubiquitin-associated protein 1
Synonyms
  • LOC362502
  • UBAP
Biotype
protein coding gene
Automated Description
Predicted to enable ubiquitin binding activity. Predicted to be involved in ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway. Predicted to be located in cytosol; intracellular membrane-bounded organelle; and plasma membrane. Predicted to be part of ESCRT I complex. Human ortholog(s) of this gene implicated in hereditary spastic paraplegia 80. Orthologous to human UBAP1 (ubiquitin associated protein 1).
RGD Description
Predicted to enable ubiquitin binding activity. Predicted to be involved in ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway. Predicted to be located in cytosol; intracellular membrane-bounded organelle; and plasma membrane. Predicted to be part of ESCRT I complex. Human ortholog(s) of this gene implicated in hereditary spastic paraplegia 80. Orthologous to human UBAP1 (ubiquitin associated protein 1); INTERACTS WITH (+)-schisandrin B; 2,4-dinitrotoluene; 2,6-dinitrotoluene.
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR15960
Stringency:
Additional filters to further constrain the results:
Species Gene symbol Count Best Best reverse
Method
Ensembl ComparaHGNCHieranoidInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidXenbaseZFIN
Homo sapiensUBAP19 of 10YesYes  
Mus musculusUbap19 of 9YesYes   
Xenopus tropicalisubap18 of 9YesYes   
Danio rerioubap18 of 9YesYes   
Drosophila melanogasterCG104355 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
Ubap1l151238263 of 9 

Function - GO Annotations

Pathways

No data available

Phenotypes

Primary Sources
None
Other Sources
None
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
Species
Gene
Association
Disease Qualifier
Disease
Evidence
Source
Based On
References
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    Alleles and Variants

    Genome location
    Assembly version
    mRatBN7.2
    Viewer Help
    Data currently unavailable; sequence viewer under construction
    Allele/Variant Symbol
    Allele Synonyms
    Category
    Variant
    Variant type
    Molecular consequence
    Has Disease Annotations
    Has Phenotype Annotations
    NC_051340.1:g.56531563C>Tvariant
    SNP
    • intron variant
    NC_051340.1:g.56532610T>Cvariant
    SNP
    • intron variant
    NC_051340.1:g.56529620C>Avariant
    SNP
    • intron variant
    NC_051340.1:g.56530830G>Avariant
    SNP
    • intron variant
    NC_051340.1:g.56532497A>Cvariant
    SNP
    • intron variant
    NC_051340.1:g.56542843A>Gvariant
    SNP
    • intron variant
    NC_051340.1:g.56544736G>Avariant
    SNP
    • intron variant
    NC_051340.1:g.56545209A>Gvariant
    SNP
    • intron variant
    NC_051340.1:g.56547459C>Gvariant
    SNP
    • intron variant
    NC_051340.1:g.56556094A>Tvariant
    SNP
    • intron variant
    Showing 1 - 10 of 139 rows
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    Transgenic Alleles

    No data available

    Models

    No data available

    Sequence Feature Viewer

    Genome location
    Assembly version
    mRatBN7.2
    Viewer Help
    Data currently unavailable; sequence viewer under construction

    Sequence Details

    Transcript: Mode:

    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