Rattus norvegicus xylosyltransferase 2 (Xylt2), mRNA

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Homozygosity for frameshift mutations in XYLT2 result in a spondylo-ocular syndrome with bone fragility, cataracts, and hearing defects. [Am J Hum Genet. 2015]
Homozygosity for frameshift mutations in XYLT2 result in a spondylo-ocular syndrome with bone fragility, cataracts, and hearing defects.
Munns CF, Fahiminiya S, Poudel N, Munteanu MC, Majewski J, Sillence DO, Metcalf JP, Biggin A, Glorieux F, Fassier F, et al. Am J Hum Genet. 2015 Jun 4; 96(6):971-8. Epub 2015 May 28.
Xylosyltransferase II is the predominant isoenzyme which is responsible for the steady-state level of xylosyltransferase activity in human serum. [Biochem Biophys Res Commun. 2015]
Xylosyltransferase II is the predominant isoenzyme which is responsible for the steady-state level of xylosyltransferase activity in human serum.
Kuhn J, Götting C, Beahm BJ, Bertozzi CR, Faust I, Kuzaj P, Knabbe C, Hendig D. Biochem Biophys Res Commun. 2015 Apr 10; 459(3):469-74. Epub 2015 Mar 3.
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 xylosyltransferase 2 (NP_071632.2).

Protein
Protein sequence from Nucleotide coding region
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Nucleotide