Gene

pja2

Species
Danio rerio
Symbol
pja2
Name
praja ring finger ubiquitin ligase 2
Synonyms
  • si:dkey-79c1.2
Biotype
protein coding gene
Automated Description
Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in protein ubiquitination. Predicted to be located in membrane. Predicted to be active in cytoplasm. Is expressed in brain; head mesenchyme; post-vent vasculature; trunk vasculature; and yolk syncytial layer. Orthologous to several human genes including PJA2 (praja ring finger ubiquitin ligase 2).
ZFIN Description
Not Available
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR15710
Stringency:
Additional filters to further constrain the results:
Species Gene symbol Count Best Best reverse
Method
Ensembl ComparaHGNCHieranoidInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidXenbaseZFIN
Homo sapiensPJA29 of 10YesYes  
Homo sapiensPJA17 of 10NoYes  
Mus musculusPja29 of 10YesYes  
Mus musculusPja17 of 10NoYes  
Rattus norvegicusPja27 of 9YesYes   
Rattus norvegicusPja14 of 9NoYes   
Xenopus tropicalispja28 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
Other Sources
None
Phenotype Term
Annotation details
References
brain development disrupted, abnormal
embryo development disrupted, abnormal
head apoptotic, abnormal
head decreased size, abnormal
notochord morphology, abnormal
post-vent region decreased length, abnormal
post-vent region deformed, abnormal
post-vent region increased curvature, abnormal
somite shape, abnormal
whole organism increased curvature, abnormal
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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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    Transgenic Alleles

    No data available

    Models

    Model name
    Experimental condition
    Associated Human Diseases
    Associated Phenotypes
    Modifier
    Source
    WT + MO1-pja2
    has condition:
    standard conditions
    • brain development disrupted, abnormal
    • embryo development disrupted, abnormal
    ZFIN
    Showing 1 - 1 of 1 rows
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    Sequence Feature Viewer

    Genome location
    Assembly version
    GRCz11
    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