Gene

Pramel43

Species
Mus musculus
Symbol
Pramel43
Name
PRAME like 43
Synonyms
  • 100041115
  • Gm3147
Biotype
protein coding gene
Automated Description
Predicted to enable ubiquitin-like ligase-substrate adaptor activity. Predicted to be involved in proteasome-mediated ubiquitin-dependent protein catabolic process. Predicted to be part of Cul2-RING ubiquitin ligase complex. Predicted to be active in cytoplasm. Orthologous to several human genes including PRAMEF1 (PRAME family member 1); PRAMEF10 (PRAME family member 10); and PRAMEF11 (PRAME family member 11).
MGI Description
Not Available
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR14224
Stringency:
Additional filters to further constrain the results:
Species Gene symbol Count Best Best reverse
Method
Ensembl ComparaHGNCHieranoidInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidXenbaseZFIN
Homo sapiensPRAMEF133 of 10YesYes  
Homo sapiensPRAMEF43 of 10YesNo  
Homo sapiensPRAMEF13 of 10YesNo  
Homo sapiensPRAMEF23 of 10YesNo  
Homo sapiensPRAMEF203 of 10YesNo  
Homo sapiensPRAMEF73 of 10YesNo  
Homo sapiensPRAMEF273 of 10YesNo  
Homo sapiensPRAMEF53 of 10YesNo  
Homo sapiensPRAMEF123 of 10YesNo  
Homo sapiensPRAMEF93 of 10YesNo  
Homo sapiensPRAMEF113 of 10YesNo  
Homo sapiensPRAMEF63 of 10YesNo  
Homo sapiensPRAMEF173 of 10YesNo  
Homo sapiensPRAMEF263 of 10YesNo  
Homo sapiensPRAMEF83 of 10YesNo  
Homo sapiensPRAMEF253 of 10YesNo  
Homo sapiensPRAMEF103 of 10YesNo  
Homo sapiensPRAMEF153 of 10YesNo  
Homo sapiensPRAMEF193 of 10YesNo  
Homo sapiensPRAMEF333 of 10YesNo  
Homo sapiensPRAMEF183 of 10YesNo  
Rattus norvegicusPramef8-ps18 of 9YesYes   
Rattus norvegicusPramel368 of 9YesYes   
Links to orthology data in JBrowse by filter level: Stringent,  Moderate,  No filter,  Best and Best Reverse

Paralogy

Function - GO Annotations

Pathways

No data available

Phenotypes

Primary Sources
None
Other Sources
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

Alleles and Variants

Genome location
Assembly version
GRCm39
Viewer Help
94.7605M94.7610M94.7615M94.7620M94.7625M94.7630M94.7635M94.7640M
Variant Types and ConsequencesOnly variants associated to alleles are shown in the graphics above. See all variants in JBrowse.
Allele/Variant Symbol
Allele Synonyms
Category
Variant
Variant type
Molecular consequence
Has Disease Annotations
Has Phenotype Annotations
NC_000071.7:g.94761670C>Tvariant
SNP
  • intron variant
NC_000071.7:g.94761362T>Avariant
SNP
  • intron variant
NC_000071.7:g.94761398G>Avariant
SNP
  • intron variant
NC_000071.7:g.94761655T>Gvariant
SNP
  • intron variant
NC_000071.7:g.94763814C>Tvariant
SNP
  • intron variant
NC_000071.7:g.94761098C>Avariant
SNP
  • intron variant
NC_000071.7:g.94762318G>Avariant
SNP
  • intron variant
Showing 1 - 7 of 7 rows
per page

Transgenic Alleles

No data available

Models

No data available

Sequence Feature Viewer

Genome location
Assembly version
GRCm39
Viewer Help
94.7605M94.7610M94.7615M94.7620M94.7625M94.7630M94.7635M94.7640M

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