| Primary Identifier | MGI:101802 | Organism | mouse, laboratory |
| Chromosome | 13 | NCBI Gene Number | 14062 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0) Enables G protein-coupled receptor activity; G-protein alpha-subunit binding activity; and G-protein beta-subunit binding activity. Involved in several processes, including modulation of chemical synaptic transmission; negative regulation of renin secretion into blood stream; and positive regulation of intracellular signal transduction. Acts upstream of or within several processes, including dendritic cell homeostasis; regulation of interleukin-1 beta production; and thrombin-activated receptor signaling pathway. Predicted to be located in several cellular components, including endosome; platelet dense tubular network; and postsynaptic membrane. Predicted to be active in plasma membrane. Is expressed in several structures, including alimentary system; central nervous system; genitourinary system; heart; and lung. Orthologous to human F2R (coagulation factor II thrombin receptor). PHENOTYPE: Targeted mutations of this locus result in increased midgestational lethality, with up to ~50% of mutants surviving to adulthood. Gene deficiency does not affect thrombin signaling in mouse platelets but markedly attenuates thrombin signaling in mouse microvascular endothelial cells. [provided by MGI curators] |
Features --> Cross References
Canonical gene --> CDSs in specific strains.
Canonical gene --> Exons in specific strains
Canonical gene --> Strain-specific IDs, biotypes, and locations
Canonical gene --> Transcripts in specific strains.
Features --> Overlapping features
