Gene

Brix1

Species
Rattus norvegicus
Symbol
Brix1
Name
biogenesis of ribosomes BRX1
Synonyms
  • brix domain containing 2
  • brix domain-containing protein 2
Biotype
protein coding gene
Automated Description
Predicted to enable RNA binding activity. Predicted to be involved in ribosomal large subunit assembly. Predicted to be located in chromosome. Predicted to be active in nucleolus. Orthologous to human BRIX1 (biogenesis of ribosomes BRX1).
RGD Description
Predicted to enable RNA binding activity. Predicted to be involved in ribosomal large subunit assembly. Predicted to be located in chromosome. Predicted to be active in nucleolus. Orthologous to human BRIX1 (biogenesis of ribosomes BRX1); INTERACTS WITH 2,4-dinitrotoluene; 6-propyl-2-thiouracil; amitrole.
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR13634
Stringency:
Additional filters to further constrain the results:
Species Gene symbol Count Best Best reverse
Method
Ensembl ComparaHGNCHieranoidInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidXenbaseZFIN
Homo sapiensBRIX110 of 10YesYes  
Mus musculusBrix19 of 9YesYes   
Xenopus tropicalisbrix15 of 9YesYes   
Danio reriobxdc29 of 9YesYes   
Drosophila melanogasterCG115839 of 9YesYes   
Caenorhabditis elegansK12H4.38 of 9YesYes   
Saccharomyces cerevisiaeBRX19 of 9YesYes   
Links to orthology data in JBrowse by filter level: Stringent,  Moderate,  No filter,  Best and Best Reverse

Paralogy

No paralogs for the gene.

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_051337.1:g.59451245G>Avariant
    SNP
    • 3 prime UTR variant
    NC_051337.1:g.59458347G>Avariant
    SNP
    • intron variant
    NC_051337.1:g.59451024A>Gvariant
    SNP
    • 3 prime UTR variant
    NC_051337.1:g.59459490A>Cvariant
    SNP
    • intron variant
    NC_051337.1:g.59456573A>Cvariant
    SNP
    • missense variant
    NC_051337.1:g.59452015T>Avariant
    SNP
    • stop gained
    NC_051337.1:g.59456836C>Tvariant
    SNP
    • intron variant
    NC_051337.1:g.59452587G>Avariant
    SNP
    • intron variant
    NC_051337.1:g.59453488G>Avariant
    SNP
    • intron variant
    NC_051337.1:g.59452341G>Tvariant
    SNP
    • intron variant
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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

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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

    No data available

    Genetic Interactions

    No data available