This is an old revision of this page, as edited by ProteinBoxBot(talk | contribs) at 14:42, 31 May 2018(←Created page with '{{Infobox_gene}} '''Sidekick cell adhesion molecule 1''' is a protein that in humans is encoded by the SDK1 gene. <ref name="entrez"> {{cite web | title...'). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.Revision as of 14:42, 31 May 2018 by ProteinBoxBot(talk | contribs)(←Created page with '{{Infobox_gene}} '''Sidekick cell adhesion molecule 1''' is a protein that in humans is encoded by the SDK1 gene. <ref name="entrez"> {{cite web | title...')
Sidekick cell adhesion molecule 1 is a protein that in humans is encoded by the SDK1 gene.
[5]
Function
The protein encoded by this gene is a member of the immunoglobulin superfamily. The protein contains six immunoglobulin-like domains and thirteen fibronectin type III domains. Fibronectin type III domains are present in both extracellular and intracellular proteins and tandem repeats are known to contain binding sites for DNA, heparin and the cell surface. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2016].
Kaufman L, Hayashi K, Ross MJ, Ross MD, Klotman PE (July 2004). "Sidekick-1 is upregulated in glomeruli in HIV-associated nephropathy". J. Am. Soc. Nephrol. 15 (7): 1721–30. PMID15213259.
Oguri M, Kato K, Yokoi K, Yoshida T, Watanabe S, Metoki N, Yoshida H, Satoh K, Aoyagi Y, Nozawa Y, Yamada Y (January 2010). "Assessment of a polymorphism of SDK1 with hypertension in Japanese Individuals". Am. J. Hypertens. 23 (1): 70–7. doi:10.1038/ajh.2009.190. PMID19851296.
Oguri M, Kato K, Yokoi K, Yoshida T, Watanabe S, Metoki N, Yoshida H, Satoh K, Aoyagi Y, Nozawa Y, Yamada Y (January 2010). "Assessment of a polymorphism of SDK1 with hypertension in Japanese Individuals". Am. J. Hypertens. 23 (1): 70–7. doi:10.1038/ajh.2009.190. PMID19851296.
Yoshida T, Kato K, Yokoi K, Oguri M, Watanabe S, Metoki N, Yoshida H, Satoh K, Aoyagi Y, Nozawa Y, Yamada Y (April 2010). "Association of genetic variants with hemorrhagic stroke in Japanese individuals". Int. J. Mol. Med. 25 (4): 649–56. PMID20198315.
Saus E, Brunet A, Armengol L, Alonso P, Crespo JM, Fernández-Aranda F, Guitart M, Martín-Santos R, Menchón JM, Navinés R, Soria V, Torrens M, Urretavizcaya M, Vallès V, Gratacòs M, Estivill X (October 2010). "Comprehensive copy number variant (CNV) analysis of neuronal pathways genes in psychiatric disorders identifies rare variants within patients". J Psychiatr Res. 44 (14): 971–8. doi:10.1016/j.jpsychires.2010.03.007. PMID20398908.
