2jgx: Difference between revisions
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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 /> | ||
==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 19:03, 21 February 2008
|
STRUCTURE OF CCP MODULE 7 OF COMPLEMENT FACTOR H- THE AMD NOT AT RISK VARIENT (402Y)
DiseaseDisease
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 StructureAbout 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
Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)
OCACategories:
- Pages with broken file links
- 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