GO curators for mouse genes have assigned the following annotations to the gene product of Cys1. (This text reflects annotations as of Tuesday, May 21, 2013.) MGI curation of this mouse gene is considered complete, including annotations derived from the biomedical literature as of December 26, 2012. If you know of any additional information regarding this mouse gene please let us know. Please supply mouse gene symbol and a PubMed ID.Summary text based on GO annotations supported by experimental evidence in mouse
Researchers have inferred from direct assay, that the gene product of Cys1
Annotations directly to molecular function for the gene Cys1 indicate that MGI curators have found no experimental data [literature] to support further annotation to this category at this time.
References
Alcalay NI et al. (2008) Acceleration of polycystic kidney disease progression in cpk mice carrying a deletion in the homeodomain protein Cux1. Am J Physiol Renal Physiol, 295:F1725-34. (PubMed:18829740)
Cho H et al. (1991) The molecular and structural basis of hearing impairment in mice with the cpk mutant gene. Ann N Y Acad Sci, 630:262-4. (PubMed:1952600)
Hou X et al. (2002) Cystin, a novel cilia-associated protein, is disrupted in the cpk mouse model of polycystic kidney disease. J Clin Invest, 109:533-40. (PubMed:11854326)
Tao B et al. (2009) Cystin localizes to primary cilia via membrane microdomains and a targeting motif. J Am Soc Nephrol, 20:2570-80. (PubMed:19850956)