Gene

Or7g19

Species
Mus musculus
Symbol
Or7g19
Name
olfactory receptor family 7 subfamily G member 19
Synonyms
  • GA_x6K02T2PVTD-12687800-12688738
  • MOR153-1
Biotype
protein coding gene
Automated Description
Predicted to enable olfactory receptor activity. Predicted to be involved in signal transduction. Predicted to act upstream of or within G protein-coupled receptor signaling pathway and sensory perception of smell. Predicted to be located in membrane. Predicted to be active in plasma membrane. Orthologous to human OR7G3 (olfactory receptor family 7 subfamily G member 3).
MGI Description
Not Available
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR48001
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
18.850M18.852M18.854M18.856M18.858M18.860M
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_000075.7:g.18856026A>Tvariant
SNP
  • missense variant
NC_000075.7:g.18856140C>Tvariant
SNP
  • synonymous variant
NC_000075.7:g.18856405C>Tvariant
SNP
  • synonymous variant
NC_000075.7:g.18856614A>Cvariant
SNP
  • synonymous variant
NC_000075.7:g.18857317A>Cvariant
SNP
  • 3 prime UTR variant
NC_000075.7:g.18859147G>Avariant
SNP
  • 3 prime UTR variant
NC_000075.7:g.18859438G>Avariant
SNP
  • 3 prime UTR variant
NC_000075.7:g.18859847C>Tvariant
SNP
  • 3 prime UTR variant
NC_000075.7:g.18857107C>Tvariant
SNP
  • 3 prime UTR variant
NC_000075.7:g.18853882G>Avariant
SNP
  • intron variant
Showing 1 - 10 of 261 rows
per page

Transgenic Alleles

No data available

Models

No data available

Sequence Feature Viewer

Genome location
Assembly version
GRCm39
Viewer Help
18.8560M18.8561M18.8562M18.8563M18.8564M18.8565M18.8566M18.8567M18.8568M

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