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2jgx

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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==
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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]]
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[[Category: Barlow, P.N.]]
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[[Category: Barlow, P N.]]
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[[Category: Blaum, B.S.]]
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[[Category: Blaum, B S.]]
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[[Category: Deakin, J.A.]]
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[[Category: Deakin, J A.]]
[[Category: Egan, C.]]
[[Category: Egan, C.]]
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[[Category: Ferreira, V.P.]]
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[[Category: Ferreira, V P.]]
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[[Category: Herbert, A.P.]]
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[[Category: Herbert, A P.]]
[[Category: Lyon, M.]]
[[Category: Lyon, M.]]
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[[Category: Pangburn, M.K.]]
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[[Category: Pangburn, M K.]]
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[[Category: Schmidt, C.Q.]]
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[[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]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jan 23 14:38:04 2008''
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''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


2jgx

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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

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