2jgx
From Proteopedia
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STRUCTURE OF CCP MODULE 7 OF COMPLEMENT FACTOR H- THE AMD NOT AT RISK VARIENT (402Y)
Disease
Known diseases associated with this structure: Complement factor H deficiency OMIM:[134370], Factor H and factor H-like 1 OMIM:[134370], Hemolytic-uremic syndrome OMIM:[134370], Macular degeneration, age-related, 4 OMIM:[134370], Membranoproliferative glomerulonephritis with CFH deficiency OMIM:[134370]
About this Structure
2JGX is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Page seeded by OCA on Mon Nov 12 22:55:14 2007
Categories: Homo sapiens | Single protein | Barlow, P.N. | Blaum, B.S. | Deakin, J.A. | Egan, C. | Ferreira, V.P. | Herbert, A.P. | Lyon, M. | Pangburn, M.K. | Schmidt, C.Q. | Uhrin, D. | Age related macular degeneration | Age-related macular degeneration | Alternative splicing | Complement | Complement alternate pathway | Disease mutation | Factor h | Glycoprotein | Glycosaminoglycan | Immune response | Innate immunity | Polymorphism | Sushi
