Gene

OR5M8

Species
Homo sapiens
Symbol
OR5M8
Name
olfactory receptor family 5 subfamily M member 8
Synonyms
  • olfactory receptor 5M8
  • olfactory receptor OR11-194
Biotype
protein coding gene
Automated Description
Predicted to enable odorant binding activity and olfactory receptor activity. Predicted to be involved in G protein-coupled receptor signaling pathway and sensory perception of smell. Predicted to be located in plasma membrane.
RGD Description
Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR48018
Stringency:
Additional filters to further constrain the results:
Species Gene symbol Count Best Best reverse
Method
Ensembl ComparaHGNCHieranoidInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidXenbaseZFIN
Mus musculusOr5m810 of 10YesYes  
Rattus norvegicusOr5m810 of 10YesYes  
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
OR5M3130284713 of 8  
OR5M9230682683 of 8  
OR5M10329381663 of 8  
OR5M1429381663 of 8  
OR5M11529778603 of 8  
OR8U1629972563 of 8  
OR5AL1730869543 of 8  
OR8U3830171543 of 8  
OR5I1931468523 of 8  
OR5AP21030270543 of 8  
OR5B211130669533 of 8  
OR8A11230669523 of 8  
OR8I21230670513 of 8  
OR8D11330170533 of 8  
OR8D41430967523 of 8  
OR8J11530770503 of 8  
OR5B121629969543 of 8  
OR5L11730867533 of 8  
OR8U91829973562 of 8  
OR8J31930669503 of 8  
OR8G12030568513 of 8  
OR8U82129972552 of 8  
OR5L22230866513 of 8  
OR8B32330467513 of 8  
OR8K32429969523 of 8  
OR8H22530667503 of 8  
OR5B22630168513 of 8  
OR5D182730766503 of 8  
OR8G52830667503 of 8  
OR5D142930867493 of 8  
OR8B23030467513 of 8  
OR8B83130666503 of 8  
OR8K13230067513 of 8  
OR5B33329967523 of 8  
OR8H33430666493 of 8  
OR9I13530167503 of 8  
OR8K53530167503 of 8  
OR8D23629369523 of 8  
OR5AR13730770502 of 8  
OR8H13830666483 of 8  
OR5F13930668522 of 8  
OR5D164030865493 of 8  
OR9Q14130368473 of 8  
OR5B174230666473 of 8  
OR5W24330767522 of 8  
OR8B124430265503 of 8  
OR5J24530468512 of 8  
OR9G44629968473 of 8  
OR5A24730270502 of 8  
OR8B44830762503 of 8  
OR9Q24930366473 of 8  
OR5P35031167492 of 8  
OR5AK25130666463 of 8  
OR5D135230964453 of 8  
OR5P25331465472 of 8  
OR5AS15431166472 of 8  
OR5A15530866492 of 8  
OR5AU15629366512 of 8  
OR5C15730067472 of 8  
OR11L15831064442 of 8  
OR5H25930564452 of 8  
OR5H16030864442 of 8  
OR5K16130462472 of 8  
OR5K26230863442 of 8  
OR5AN16329766452 of 8  
OR6B26430364442 of 8  
OR5AC26529764462 of 8  
OR5K36630663442 of 8  
OR6Q16730961442 of 8  
OR5H156830862432 of 8  
OR5H146929965442 of 8  
OR5H66929964442 of 8  
OR6B37030363432 of 8  
OR10V17130264422 of 8  
OR14A27231160422 of 8  
OR13A17330361442 of 8  
OR5K47430161452 of 8  
OR6P17530361422 of 8  
OR14A167630062412 of 8  
OR10Q17729363422 of 8  
OR14K17830557402 of 8  
OR14C367930959382 of 8  
OR14J18030256402 of 8  
OR14I18131755382 of 8  
OR10W18229656362 of 8  
OR5AK3P833 of 8  
OR8G2P833 of 8  
OR8J2842 of 8  
OR5AC1842 of 8  
OR8G3842 of 8  
OR5G3842 of 8  
OR5D3P842 of 8  

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
Species
Gene
Association
Disease Qualifier
Disease
Evidence
Source
Based On
References
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    Alleles and Variants

    Genome location
    Assembly version
    GRCh38
    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_000011.10:g.56491090G>Avariant
    SNP
    • missense variant
    NC_000011.10:g.56491124T>Cvariant
    SNP
    • missense variant
    NC_000011.10:g.56491315C>Tvariant
    SNP
    • missense variant
    NC_000011.10:g.56490476C>Tvariant
    SNP
    • missense variant
    NC_000011.10:g.56490898T>Cvariant
    SNP
    • missense variant
    NC_000011.10:g.56490586G>Tvariant
    SNP
    • missense variant
    NC_000011.10:g.56490613G>Tvariant
    SNP
    • missense variant
    NC_000011.10:g.56491217C>Gvariant
    SNP
    • missense variant
    NC_000011.10:g.56490677C>Gvariant
    SNP
    • missense variant
    NC_000011.10:g.56490701T>Gvariant
    SNP
    • missense variant
    Showing 1 - 10 of 25 rows
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    Transgenic Alleles

    No data available

    Models

    No data available

    Sequence Feature Viewer

    Genome location
    Assembly version
    GRCh38
    Viewer Help
    Data currently unavailable; sequence viewer under construction

    Sequence Details

    Transcript: Mode:

    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

    4 interactor genes based on 4 annotations
    OR5M8 molecule type
    Interactor gene
    Interactor species
    Interactor molecule type
    Detection methods
    Source
    Reference
    protein
    CFTRHomo sapiens
    protein
    • protein complementation assay
    PMID:35156780
    protein
    RNF181Homo sapiens
    protein
    • affinity chromatography technology
    PMID:33961781
    protein
    UBE3AHomo sapiens
    protein
    • affinity chromatography technology
    PMID:33961781
    protein
    UNC45BHomo sapiens
    protein
    • affinity chromatography technology
    PMID:33961781
    Showing 1 - 4 of 4 rows
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    Genetic Interactions

    No data available