PREDICTED: Rattus norvegicus potassium channel tetramerization domain - Nucleotide

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A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystonia. [Am J Hum Genet. 2015]
A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystonia.
Mencacci NE, Rubio-Agusti I, Zdebik A, Asmus F, Ludtmann MH, Ryten M, Plagnol V, Hauser AK, Bandres-Ciga S, Bettencourt C, et al. Am J Hum Genet. 2015 Jun 4; 96(6):938-47. Epub 2015 May 14.
Ubiquitin-proteasome system controls ciliogenesis at the initial step of axoneme extension. [Nat Commun. 2014]
Ubiquitin-proteasome system controls ciliogenesis at the initial step of axoneme extension.
Kasahara K, Kawakami Y, Kiyono T, Yonemura S, Kawamura Y, Era S, Matsuzaki F, Goshima N, Inagaki M. Nat Commun. 2014 Oct 1; 5:5081. Epub 2014 Oct 1.
Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium. [Brief Bioinform. 2011]
Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium.
Gaudet P, Livstone MS, Lewis SE, Thomas PD. Brief Bioinform. 2011 Sep; 12(5):449-62. Epub 2011 Aug 27.

RefSeq protein product
See the reference protein sequence for BTB/POZ domain-containing protein KCTD17 isoform X7 (XP_038934880.1).

PREDICTED: Rattus norvegicus potassium channel tetramerization domain containing...
PREDICTED: Rattus norvegicus potassium channel tetramerization domain containing 17 (Kctd17), transcript variant X7, mRNA
gi|2678957179|ref|XM_039078952.2|

Nucleotide
PREDICTED: Homo sapiens SMG1 nonsense mediated mRNA decay associated PI3K relate...
PREDICTED: Homo sapiens SMG1 nonsense mediated mRNA decay associated PI3K related kinase (SMG1), transcript variant X4, mRNA
gi|2462548007|ref|XM_054379837.1|

Nucleotide
Retroviruses
Retroviruses

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Nucleotide