ITGA2, integrin subunit alpha 2, 3673

N. diseases: 166; N. variants: 7
Disease: Glycoprotein IA Deficiency ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3280114
Disease: Glycoprotein IA Deficiency
Glycoprotein IA Deficiency 		0.500 Biomarker disease GENOMICS_ENGLAND A point mutation Thr(799)Met on the alpha(2) integrin leads to the formation of new human platelet alloantigen Sit(a) and affects collagen-induced aggregation. 10590055 1999
CUI: C3280114
Disease: Glycoprotein IA Deficiency
Glycoprotein IA Deficiency 		0.500 Biomarker disease CTD_human