dynein cytoplasmic 2 light intermediate chain 1 [Rattus norvegicus]

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DYNC2LI1 mutations broaden the clinical spectrum of dynein-2 defects. [Sci Rep. 2015]
DYNC2LI1 mutations broaden the clinical spectrum of dynein-2 defects.
Kessler K, Wunderlich I, Uebe S, Falk NS, Gießl A, Brandstätter JH, Popp B, Klinger P, Ekici AB, Sticht H, et al. Sci Rep. 2015 Jul 1; 5:11649. Epub 2015 Jul 1.
Mutations in DYNC2LI1 disrupt cilia function and cause short rib polydactyly syndrome. [Nat Commun. 2015]
Mutations in DYNC2LI1 disrupt cilia function and cause short rib polydactyly syndrome.
Taylor SP, Dantas TJ, Duran I, Wu S, Lachman RS, University of Washington Center for Mendelian Genomics Consortium, Nelson SF, Cohn DH, Vallee RB, Krakow D. Nat Commun. 2015 Jun 16; 6:7092. Epub 2015 Jun 16.
Recombinant human cytoplasmic dynein heavy chain 1 and 2: observation of dynein-2 motor activity in vitro. [FEBS Lett. 2011]
Recombinant human cytoplasmic dynein heavy chain 1 and 2: observation of dynein-2 motor activity in vitro.
Ichikawa M, Watanabe Y, Murayama T, Toyoshima YY. FEBS Lett. 2011 Aug 4; 585(15):2419-23. Epub 2011 Jun 26.

RefSeq protein
See the reference protein sequence for cytoplasmic dynein 2 light intermediate chain 1 (NP_001382012.1).

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Protein