Version: 8.0.0
Date: Tue Jan 28 2025
6430548M08Rikl
Rattus norvegicusRGD:1304884
SummaryOrthologyParalogyFunction - GO AnnotationsPathwaysPhenotypesDisease AssociationsAlleles and VariantsTransgenic AllelesModelsSequence Feature ViewerSequence DetailsExpressionMolecular InteractionsGenetic Interactions
Gene

6430548M08Rikl

Species
Rattus norvegicus
Symbol
6430548M08Rikl
Name
RIKEN cDNA 6430548M08 gene like
Synonyms
  • hypothetical protein LOC307907
  • Kiaa0513
Biotype
protein coding gene
Automated Description
Orthologous to human KIAA0513 (KIAA0513).
RGD Description
Orthologous to human KIAA0513 (KIAA0513); INTERACTS WITH 2,3,7,8-tetrachlorodibenzodioxine; 6-propyl-2-thiouracil; acetamide.
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR13663
Stringency:
Additional filters to further constrain the results:
Species Gene symbol Count Best Best reverse
Method
Ensembl ComparaHGNCHieranoidInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidXenbaseZFIN
Homo sapiensKIAA051310 of 10YesYes☑☑☑☑☑☑☑☑☑☑  
Mus musculus6430548M08Rik9 of 9YesYes☑ ☑☑☑☑☑☑☑☑  
Xenopus tropicalisKIAA05139 of 9YesYes☑ ☑☑☑☑☑☑☑☑  
Danio reriokiaa05139 of 9YesYes☑ ☑☑☑☑☑☑☑☑  
Drosophila melanogasterCG173788 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_051354.1:g.48198722T>Cvariant
    SNP
    • synonymous variant
    NC_051354.1:g.48178825G>Avariant
    SNP
    • intron variant
    NC_051354.1:g.48179585T>Cvariant
    SNP
    • intron variant
    NC_051354.1:g.48174492T>Cvariant
    SNP
    • intron variant
    NC_051354.1:g.48174888T>Cvariant
    SNP
    • intron variant
    NC_051354.1:g.48178044G>Avariant
    SNP
    • intron variant
    NC_051354.1:g.48179463C>Avariant
    SNP
    • intron variant
    NC_051354.1:g.48168713C>Gvariant
    SNP
    • 5 prime UTR variant
    NC_051354.1:g.48169895T>Cvariant
    SNP
    • intron variant
    NC_051354.1:g.48170686T>Cvariant
    SNP
    • intron variant
    Showing 1 - 10 of 126 rows
    per page
    View detailed Alleles/Variants information
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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