2jgx
From Proteopedia
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caption="2jgx" /> | caption="2jgx" /> | ||
'''STRUCTURE OF CCP MODULE 7 OF COMPLEMENT FACTOR H- THE AMD NOT AT RISK VARIENT (402Y)'''<br /> | '''STRUCTURE OF CCP MODULE 7 OF COMPLEMENT FACTOR H- THE AMD NOT AT RISK VARIENT (402Y)'''<br /> | ||
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| + | ==Disease== | ||
| + | Known diseases associated with this structure: Complement factor H deficiency OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134370 134370]], Factor H and factor H-like 1 OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134370 134370]], Hemolytic-uremic syndrome OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134370 134370]], Macular degeneration, age-related, 4 OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134370 134370]], Membranoproliferative glomerulonephritis with CFH deficiency OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134370 134370]] | ||
==About this Structure== | ==About this Structure== | ||
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[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Single protein]] | [[Category: Single protein]] | ||
| - | [[Category: Barlow, P | + | [[Category: Barlow, P N.]] |
| - | [[Category: Blaum, B | + | [[Category: Blaum, B S.]] |
| - | [[Category: Deakin, J | + | [[Category: Deakin, J A.]] |
[[Category: Egan, C.]] | [[Category: Egan, C.]] | ||
| - | [[Category: Ferreira, V | + | [[Category: Ferreira, V P.]] |
| - | [[Category: Herbert, A | + | [[Category: Herbert, A P.]] |
[[Category: Lyon, M.]] | [[Category: Lyon, M.]] | ||
| - | [[Category: Pangburn, M | + | [[Category: Pangburn, M K.]] |
| - | [[Category: Schmidt, C | + | [[Category: Schmidt, C Q.]] |
[[Category: Uhrin, D.]] | [[Category: Uhrin, D.]] | ||
[[Category: age related macular degeneration]] | [[Category: age related macular degeneration]] | ||
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[[Category: sushi]] | [[Category: sushi]] | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 18:03:08 2008'' |
Revision as of 16:03, 21 February 2008
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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 Thu Feb 21 18:03:08 2008
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
