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GENATLAS PHENOTYPE

last update : 5/09/2006

Symbol	P2RY12
Location	3q24-q25
Name	platelet ADP receptor defect
Other name(s)	bleeding disorder due to P2RY12 defect
Corresponding gene	P2RY12
Main clinical features	bleeding disorder linked to a defective interaction between ADP (adenine diphosphate) and its receptor on platelets and a secundary defect of GP2B/GPRA function, with reduced capacity of platelets to bind to each other in response to ADP
Genetic determination
Function/system disorder	hematology
Type	disease

Gene product

Name	purinoreceptor P2Y12