Compare GO annotations related to Bleeding disorder due to P2RY12 defect using OMIM genes and OrthoDisease orthologs

A table of the annotations represented in this image is provided below.
CategoryIDTermDB ObjectEvidenceOrganismReference
Molecular FunctionGO:0001609adenosine receptor activity, G-protein coupled MGI:1918089IMPMouseMGI:MGI:2136079|PMID:11413167
Molecular FunctionGO:0001621platelet ADP receptor activity MGI:1918089IMPMouseMGI:MGI:2136079|PMID:11413167
Molecular FunctionGO:0001621platelet ADP receptor activity RGD:621681IDARatRGD:633493|PMID:11196645
Cellular ComponentGO:0005886plasma membrane RGD:621681IMPRatRGD:633493|PMID:11196645
Biological ProcessGO:0007186G-protein coupled receptor protein signaling pathway RGD:621681IMPRatRGD:633493|PMID:11196645
Biological ProcessGO:0007188G-protein signaling, coupled to cAMP nucleotide second messenger MGI:1918089IMPMouseMGI:MGI:2136079|PMID:11413167
Biological ProcessGO:0030168platelet activation MGI:1918089IMPMouseMGI:MGI:2136079|PMID:11413167
Biological ProcessGO:0043491protein kinase B signaling cascade RGD:621681IMPRatRGD:1580185|PMID:15056287