Version: 8.0.0Date: Tue Jan 28 2025
Gene
Gpr87
- Species
- Rattus norvegicus
- Symbol
- Gpr87
- Name
- G protein-coupled receptor 87
- Synonyms
- G-protein coupled receptor 87
- LOC310443
- Biotype
- protein coding gene
- Automated Description
- Predicted to enable G protein-coupled purinergic nucleotide receptor activity. Predicted to be involved in G protein-coupled receptor signaling pathway. Predicted to be located in plasma membrane. Orthologous to human GPR87 (G protein-coupled receptor 87).
- RGD Description
- Predicted to enable G protein-coupled purinergic nucleotide receptor activity. Predicted to be involved in G protein-coupled receptor signaling pathway. Predicted to be located in plasma membrane. Orthologous to human GPR87 (G protein-coupled receptor 87); INTERACTS WITH 17beta-estradiol; 17beta-estradiol 3-benzoate; bisphenol A.
- Cross References
- Additional Information
- Literature
Orthology
- Gene tree
- PANTHER:PTHR24233
Stringency:
Additional filters to further constrain the results:
Links to orthology data in JBrowse by filter level: Stringent, Moderate, No filter, Best and Best Reverse
Paralogy
| Gene symbol | Rank | Alignment Length (aa) | Similarity % | Identity % | Method Count | Method Ensembl ComparaHGNCInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidSGD |
|---|---|---|---|---|---|---|
| P2ry14 | 1 | 311 | 66 | 48 | 3 of 9 | ☑☐☐☐☐☐☑☑☐ |
| P2ry12 | 2 | 306 | 63 | 43 | 3 of 9 | ☑☐☐☐☐☐☑☑☐ |
| P2ry13 | 3 | 307 | 62 | 40 | 3 of 9 | ☑☐☐☐☐☐☑☑☐ |
| Gpr34 | 4 | 314 | 50 | 32 | 3 of 9 | ☑☐☐☐☐☐☑☑☐ |
| Ptafr | 5 | 326 | 48 | 28 | 3 of 9 | ☑☐☐☐☐☐☑☑☐ |
| Gpr171 | 6 | 308 | 51 | 30 | 3 of 9 | ☑☐☐☐☐☐☑☑☐ |
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 |
|---|---|---|---|---|---|---|---|---|
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Alleles and Variants
- Genome location
- Chr2:143439735...143458190 - (18.46 kb)
- Assembly version
- mRatBN7.2
- 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 |
|---|---|---|---|---|---|---|---|
| NC_051337.1:g.143456758C>T | variant | SNP
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| NC_051337.1:g.143449698T>C | variant | SNP
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| NC_051337.1:g.143453249G>A | variant | SNP
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| NC_051337.1:g.143453484G>T | variant | SNP
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| NC_051337.1:g.143453592A>T | variant | SNP
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| NC_051337.1:g.143453930T>G | variant | SNP
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| NC_051337.1:g.143454069T>C | variant | SNP
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| NC_051337.1:g.143454860A>C | variant | SNP
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| NC_051337.1:g.143450855T>C | variant | SNP
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| NC_051337.1:g.143452648C>T | variant | SNP
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Sequence Feature Viewer
- Genome location
- Chr2:143439735...143458190 - (18.46 kb)
- Assembly version
- mRatBN7.2
- Viewer Help
Data currently unavailable; sequence viewer under construction