Gene Symbol: Dync2li1
Description: dynein cytoplasmic 2 light intermediate chain 1
Alias: 4933404O11Rik, CGI-60, D2lic, LIC3, mD2LIC, cytoplasmic dynein 2 light intermediate chain 1, dynein 2 light intermediate chain
Perrone C, Tritschler D, Taulman P, Bower R, Yoder B, Porter M. A novel dynein light intermediate chain colocalizes with the retrograde motor for intraflagellar transport at sites of axoneme assembly in chlamydomonas and Mammalian cells. Mol Biol Cell. 2003;14:2041-56 pubmed
..Recent work identified a novel dynein light intermediate chain (D2LIC) that colocalized with the mammalian cDHC1b homolog DHC2 in the centrosomal region of cultured cells...
Rana A, Barbera J, Rodriguez T, Lynch D, Hirst E, Smith J, et al
. Targeted deletion of the novel cytoplasmic dynein mD2LIC disrupts the embryonic organiser, formation of the body axes and specification of ventral cell fates. Development. 2004;131:4999-5007 pubmed
..In this paper, we study the recently discovered mouse dynein 2 light intermediate chain (mD2LIC), which is believed to be involved in retrograde intraflagella transport and which, like ..
Smith S, Qu H, Taleb N, Kishimoto N, Scheel D, Lu Y, et al
. Rfx6 directs islet formation and insulin production in mice and humans. Nature. 2010;463:775-80 pubmed publisher
..These studies demonstrate a unique position for Rfx6 in the hierarchy of factors that coordinate pancreatic islet development in both mice and humans. Rfx6 could prove useful in efforts to generate beta-cells for patients with diabetes. ..
Goggolidou P, Stevens J, Agueci F, Keynton J, Wheway G, Grimes D, et al
. ATMIN is a transcriptional regulator of both lung morphogenesis and ciliogenesis. Development. 2014;141:3966-77 pubmed publisher
..This identifies potential novel components of cytoplasmic dynein 2 and furthermore provides fresh insights into the molecular pathogenesis of human skeletal ciliopathies. ..
Hai Q, Ritchey B, Robinet P, Alzayed A, Brubaker G, Zhang J, et al
. Quantitative Trait Locus Mapping of Macrophage Cholesterol Metabolism and CRISPR/Cas9 Editing Implicate an ACAT1 Truncation as a Causal Modifier Variant. Arterioscler Thromb Vasc Biol. 2018;38:83-91 pubmed publisher
..A Soat1 deletion present in AKR mice, and resultant N-terminal ACAT1 truncation, was confirmed to be a significant modifier of macrophage cholesterol metabolism. Other Mcmm loci candidate genes were prioritized via bioinformatics. ..
Pfister K, Fisher E, Gibbons I, Hays T, Holzbaur E, McIntosh J, et al
. Cytoplasmic dynein nomenclature. J Cell Biol. 2005;171:411-3 pubmed
..This nomenclature recognizes the two distinct cytoplasmic dynein complexes and has the flexibility to accommodate the discovery of new subunits and isoforms. ..
Hossain Z, Ali S, Ko H, Xu J, Ng C, Guo K, et al
. Glomerulocystic kidney disease in mice with a targeted inactivation of Wwtr1. Proc Natl Acad Sci U S A. 2007;104:1631-6 pubmed
..Thus, Wwtr1 is critical for the integrity of renal cilia and its absence in mice leads to the development of renal cysts, indicating that Wwtr1 may represent a candidate gene for polycystic kidney disease in humans. ..
Bonnafe E, Touka M, AitLounis A, Baas D, Barras E, Ucla C, et al
. The transcription factor RFX3 directs nodal cilium development and left-right asymmetry specification. Mol Cell Biol. 2004;24:4417-27 pubmed
..Finally, we show that RFX3 regulates the expression of D2lic, the mouse orthologue of a Caenorhabditis elegans gene that is implicated in intraflagellar transport, a process ..