Version: 8.0.0
Date: Tue Jan 28 2025
Tmem218
Rattus norvegicusRGD:1311364
SummaryOrthologyParalogyFunction - GO AnnotationsPathwaysPhenotypesDisease AssociationsAlleles and VariantsTransgenic AllelesModelsSequence Feature ViewerSequence DetailsExpressionMolecular InteractionsGenetic Interactions
Gene

Tmem218

Species
Rattus norvegicus
Symbol
Tmem218
Name
transmembrane protein 218
Synonyms
  • LOC300516
  • MGC105984
Biotype
protein coding gene
Automated Description
Predicted to be located in cilium and membrane. Human ortholog(s) of this gene implicated in Joubert syndrome. Orthologous to human TMEM218 (transmembrane protein 218).
RGD Description
Predicted to be located in cilium and membrane. Human ortholog(s) of this gene implicated in Joubert syndrome. Orthologous to human TMEM218 (transmembrane protein 218); INTERACTS WITH (+)-schisandrin B; 17beta-estradiol; 2,3,7,8-tetrachlorodibenzodioxine.
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR31622
Stringency:
Additional filters to further constrain the results:
Species Gene symbol Count Best Best reverse
Method
Ensembl ComparaHGNCHieranoidInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidXenbaseZFIN
Homo sapiensTMEM21810 of 10YesYes☑☑☑☑☑☑☑☑☑☑  
Mus musculusTmem2189 of 9YesYes☑ ☑☑☑☑☑☑☑☑  
Xenopus tropicalistmem2189 of 9YesYes☑ ☑☑☑☑☑☑☑☑  
Danio reriotmem2189 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_051343.1:g.36934466C>Tvariant
    SNP
    • intron variant
    NC_051343.1:g.36935403C>Tvariant
    SNP
    • intron variant
    NC_051343.1:g.36937493G>Cvariant
    SNP
    • intron variant
    NC_051343.1:g.36935445G>Avariant
    SNP
    • intron variant
    NC_051343.1:g.36935774A>Gvariant
    SNP
    • intron variant
    NC_051343.1:g.36928048T>Avariant
    SNP
    • intron variant
    NC_051343.1:g.36928259C>Tvariant
    SNP
    • intron variant
    NC_051343.1:g.36927620T>Cvariant
    SNP
    • intron variant
    NC_051343.1:g.36931988A>Gvariant
    SNP
    • intron variant
    NC_051343.1:g.36932422T>Cvariant
    SNP
    • intron variant
    Showing 1 - 10 of 46 rows
    per page
    View detailed Alleles/Variants information
    Download all Alleles/Variants for all genes of the species

    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