2edu: Difference between revisions

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|ACTIVITY=  
|ACTIVITY=  
|GENE= KIF22 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
|GENE= KIF22 ([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=2edu FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2edu OCA], [http://www.ebi.ac.uk/pdbsum/2edu PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2edu RCSB]</span>
}}
}}


'''Solution structure of RSGI RUH-070, a C-terminal domain of kinesin-like protein KIF22 from human cDNA'''
'''Solution structure of RSGI RUH-070, a C-terminal domain of kinesin-like protein KIF22 from human cDNA'''


==Disease==
Known diseases associated with this structure: Bart-Pumphrey syndrome OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=121011 121011]], Deafness, autosomal dominant 3 OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=121011 121011]], Deafness, autosomal recessive 1 OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=121011 121011]], Hystrix-like ichthyosis with deafness OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=121011 121011]], Keratitis-ichthyosis-deafness syndrome OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=121011 121011]], Keratoderma, palmoplantar, with deafness OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=121011 121011]], Vohwinkel syndrome OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=121011 121011]]


==About this Structure==
==About this Structure==
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[[Category: transport protein]]
[[Category: transport protein]]


''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 16:38:46 2008''
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