Gene

Gpr162

Species
Rattus norvegicus
Symbol
Gpr162
Name
G protein-coupled receptor 162
Synonyms
  • gene rich cluster, A
  • gene rich cluster, A gene
Biotype
protein coding gene
Automated Description
Predicted to enable G protein-coupled receptor activity. Predicted to be involved in G protein-coupled receptor signaling pathway. Predicted to be located in membrane. Orthologous to human GPR162 (G protein-coupled receptor 162).
RGD Description
Predicted to enable G protein-coupled receptor activity. Predicted to be involved in G protein-coupled receptor signaling pathway. Predicted to be located in membrane. Orthologous to human GPR162 (G protein-coupled receptor 162); INTERACTS WITH 2,3,7,8-tetrachlorodibenzodioxine; bisphenol A; C60 fullerene.
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR16518
Stringency:
Additional filters to further constrain the results:
Species Gene symbol Count Best Best reverse
Method
Ensembl ComparaHGNCHieranoidInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidXenbaseZFIN
Homo sapiensGPR1629 of 10YesYes  
Mus musculusGpr1629 of 9YesYes   
Xenopus tropicalisgpr1628 of 9YesYes   
Links to orthology data in JBrowse by filter level: Stringent,  Moderate,  No filter,  Best and Best Reverse

Paralogy

Gene symbolRank Alignment Length (aa) Similarity %Identity %Method Count
Method
Ensembl ComparaHGNCInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidSGD
Gpr153166156453 of 9 

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

Alleles and Variants

No mapped variant information available
Allele/Variant Symbol
Allele Synonyms
Category
Variant
Variant type
Molecular consequence
Has Disease Annotations
Has Phenotype Annotations
NC_051339.1:g.157663860C>Tvariant
SNP
  • intron variant
NC_051339.1:g.157662402G>Avariant
SNP
  • 3 prime UTR variant
NC_051339.1:g.157663764T>Cvariant
SNP
  • intron variant
NC_051339.1:g.157667757G>Avariant
SNP
  • intron variant
NC_051339.1:g.157663796T>Cvariant
SNP
  • intron variant
NC_051339.1:g.157666354A>Gvariant
SNP
  • intron variant
NC_051339.1:g.157663780C>Tvariant
SNP
  • intron variant
NC_051339.1:g.157663792T>Cvariant
SNP
  • intron variant
NC_051339.1:g.157665504G>Avariant
SNP
  • synonymous variant
NC_051339.1:g.157664621C>Tvariant
SNP
  • intron variant
Showing 1 - 10 of 10 rows
per page

Transgenic Alleles

No data available

Models

No data available

Sequence Feature Viewer

Genome location
Assembly version
mRatBN7.2
Viewer Help
157.663M157.664M157.665M157.666M157.667M157.668M

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