2dib: Difference between revisions

From Proteopedia
Jump to navigationJump to search
← Older editNewer edit →
OCA (talk | contribs)
Bots, Bureaucrats, journal, Administrators
3,328,572 edits
No edit summary
OCA (talk | contribs)
Bots, Bureaucrats, journal, Administrators
3,328,572 edits
No edit summary
Line 14: Line 14:


==Disease==
==Disease==
Known disease associated with this structure: Atelosteogenesis, type III OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603381 603381]], Atelostogenesis, type I OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603381 603381]], Boomerang dysplasia OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603381 603381]], Larson syndrome OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603381 603381]], Spondylocarpotarsal synostosis syndrome OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603381 603381]]
Known disease associated with this structure: Atelosteogenesis, type III OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603381 603381]], Atelostogenesis, type I OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603381 603381]], Boomerang dysplasia OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603381 603381]], Larsen syndrome OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603381 603381]], Spondylocarpotarsal synostosis syndrome OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603381 603381]]


==About this Structure==
==About this Structure==
Line 35: Line 35:
[[Category: Structural genomic]]
[[Category: Structural genomic]]


''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Nov 16 15:56:33 2008''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Feb 17 00:58:43 2009''

Revision as of 22:58, 16 February 2009

File:2dib.png

Template:STRUCTURE 2dib

Solution structure of the 11th filamin domain from human Filamin-B

Disease

Known disease associated with this structure: Atelosteogenesis, type III OMIM:[603381], Atelostogenesis, type I OMIM:[603381], Boomerang dysplasia OMIM:[603381], Larsen syndrome OMIM:[603381], Spondylocarpotarsal synostosis syndrome OMIM:[603381]

About this Structure

2DIB is a 1 chain structure of sequence from Homo sapiens. Full experimental information is available from OCA.

Page seeded by OCA on Tue Feb 17 00:58:43 2009

Proteopedia Page Contributors and Editors (what is this?)

OCA

Retrieved from "https://proteopedia.org/index.php?title=2dib&oldid=860466"