2dlg

@@ Line 7: / Line 7: @@
 |ACTIVITY=
 |GENE= FLNB, FLN1L, FLN3, TABP, TAP ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
+|DOMAIN=
+|RELATEDENTRY=
+|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2dlg FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2dlg OCA], [http://www.ebi.ac.uk/pdbsum/2dlg PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2dlg RCSB]</span>
 }}
 '''Solution structure of the 20th Filamin domain from human Filamin-B'''
-==Disease==
-Known diseases 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]], Bare lymphocyte syndrome, type I OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=170260 170260]], 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]]
 ==About this Structure==
@@ Line 35: / Line 35: @@
 [[Category: structural genomic]]
-''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 16:28:32 2008''
+''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 02:36:11 2008''

Revision as of 23:36, 30 March 2008