Version: 8.0.0
Date: Tue Jan 28 2025
Rimoc1
Mus musculusMGI:2146232
SummaryOrthologyParalogyFunction - GO AnnotationsPathwaysPhenotypesDisease AssociationsAlleles and VariantsTransgenic AllelesModelsSequence Feature ViewerSequence DetailsExpressionMolecular InteractionsGenetic Interactions
Gene

Rimoc1

Species
Mus musculus
Symbol
Rimoc1
Name
RAB7A interacting MON1-CCZ1 complex subunit 1
Synonyms
  • AI195826
  • AW549877
Biotype
protein coding gene
Automated Description
Predicted to be involved in mitophagy. Predicted to be located in cytosol and nucleoplasm. Is expressed in several structures, including adipose tissue; ganglia; gut; hemolymphoid system; and male reproductive gland or organ. Orthologous to human RIMOC1 (RAB7A interacting MON1-CCZ1 complex subunit 1).
MGI Description
Not Available
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR28494
Stringency:
Additional filters to further constrain the results:
Species Gene symbol Count Best Best reverse
Method
Ensembl ComparaHGNCHieranoidInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidXenbaseZFIN
Homo sapiensRIMOC110 of 10YesYes☑☑☑☑☑☑☑☑☑☑  
Rattus norvegicusRimoc19 of 9YesYes☑ ☑☑☑☑☑☑☑☑  
Danio reriorimoc110 of 10YesYes☑ ☑☑☑☑☑☑☑☑ ☑
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

No function available for that gene

Pathways

No data available

Phenotypes

Primary Sources
Other Sources
Phenotype Term
Annotation details
References
abnormal retina blood vessel morphology
abnormal retina inner nuclear layer morphology
abnormal retina outer nuclear layer morphology
decreased total retina thickness
increased body temperature
increased bone mineral density
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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
No records match query. Try removing filters.
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    Alleles and Variants

    Genome location
    Assembly version
    GRCm39
    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
    Rimoc1tm1a(EUCOMM)Wtsiallele
    Rimoc1tm1b(EUCOMM)Wtsiallele
    		Yes
    Rimoc1em1Smoc
    • AW549877em1Smoc
    		allele
    NC_000081.7:g.4017255A>Cvariant
    SNP
    • intron variant
    NC_000081.7:g.4016226G>Tvariant
    SNP
    • intron variant
    NC_000081.7:g.4016268A>Tvariant
    SNP
    • intron variant
    NC_000081.7:g.4017428G>Cvariant
    SNP
    • intron variant
    NC_000081.7:g.4018819C>Avariant
    SNP
    • intron variant
    NC_000081.7:g.4020208C>Gvariant
    SNP
    • intron variant
    NC_000081.7:g.4021401A>Tvariant
    SNP
    • intron variant
    Showing 1 - 10 of 259 rows
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    View detailed Alleles/Variants information
    Download all Alleles/Variants for all genes of the species

    Transgenic Alleles

    No data available

    Models

    Model name
    Experimental condition
    Associated Human Diseases
    Associated Phenotypes
    Modifier
    Source
    Rimoc1tm1b(EUCOMM)Wtsi/Rimoc1tm1b(EUCOMM)Wtsi [background:] C57BL/6N-Rimoc1tm1b(EUCOMM)Wtsi/Bay
    • abnormal retina blood vessel morphology
    • abnormal retina inner nuclear layer morphology
    		MGI
    Showing 1 - 1 of 1 rows
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    Sequence Feature Viewer

    Genome location
    Assembly version
    GRCm39
    Viewer Help
    Data currently unavailable; sequence viewer under construction

    Sequence Details

    Loading...

    Expression

    Primary Sources
    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