Gene

Zfp831

Species
Mus musculus
Symbol
Zfp831
Name
zinc finger protein 831
Synonyms
  • ENSMUSG00000050600
  • OTTMUSG00000017459
Biotype
protein coding gene
Automated Description
Is expressed in brain; gut gland; and testis. Orthologous to human ZNF831 (zinc finger protein 831).
MGI Description
Not Available
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR47166
Stringency:
Additional filters to further constrain the results:
Species Gene symbol Count Best Best reverse
Method
Ensembl ComparaHGNCHieranoidInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidXenbaseZFIN
Homo sapiensZNF83110 of 10YesYes  
Rattus norvegicusZfp8319 of 9YesYes   
Xenopus tropicalisznf8318 of 9YesYes   
Danio rerioznf8317 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

Pathways

No data available

Phenotypes

Primary Sources
Other Sources
Phenotype Term
Annotation details
References
abnormal coat appearance
abnormal skin coloration
short tibia
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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
    Zfp831tm1b(KOMP)Wtsiallele
    Yes
    Zfp831tm1a(KOMP)Wtsiallele
    Zfp831em1Cdon
    • Zfp831-
    allele
    Zfp831em2Cdon
    • Zfp831flag
    allele
    NC_000068.8:g.174443673A>Gvariant
    SNP
    • intron variant
    NC_000068.8:g.174443679G>Avariant
    SNP
    • intron variant
    NC_000068.8:g.174449678A>Cvariant
    SNP
    • intron variant
    NC_000068.8:g.174450330G>Avariant
    SNP
    • intron variant
    NC_000068.8:g.174450792A>Cvariant
    SNP
    • intron variant
    NC_000068.8:g.174446892C>Avariant
    SNP
    • intron variant
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    Transgenic Alleles

    No data available

    Models

    Model name
    Experimental condition
    Associated Human Diseases
    Associated Phenotypes
    Modifier
    Source
    Zfp831tm1b(KOMP)Wtsi/Zfp831tm1b(KOMP)Wtsi [background:] C57BL/6N-Zfp831tm1b(KOMP)Wtsi/Bay
    • abnormal coat appearance
    • abnormal skin coloration
    MGI
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    Sequence Feature Viewer

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

    Sequence Details

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    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