transportin-3 isoform X3 [Rattus norvegicus]

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Novel mutation in TNPO3 causes congenital limb-girdle myopathy with slow progression. [Neurol Genet. 2019]
Novel mutation in TNPO3 causes congenital limb-girdle myopathy with slow progression.
Vihola A, Palmio J, Danielsson O, Penttilä S, Louiselle D, Pittman S, Weihl C, Udd B. Neurol Genet. 2019 Jun; 5(3):e337. Epub 2019 May 2.
The mutation of Transportin 3 gene that causes limb girdle muscular dystrophy 1F induces protection against HIV-1 infection. [PLoS Pathog. 2019]
The mutation of Transportin 3 gene that causes limb girdle muscular dystrophy 1F induces protection against HIV-1 infection.
Rodríguez-Mora S, De Wit F, García-Perez J, Bermejo M, López-Huertas MR, Mateos E, Martí P, Rocha S, Vigón L, Christ F, et al. PLoS Pathog. 2019 Aug; 15(8):e1007958. Epub 2019 Aug 29.
Differential role for phosphorylation in alternative polyadenylation function versus nuclear import of SR-like protein CPSF6. [Nucleic Acids Res. 2019]
Differential role for phosphorylation in alternative polyadenylation function versus nuclear import of SR-like protein CPSF6.
Jang S, Cook NJ, Pye VE, Bedwell GJ, Dudek AM, Singh PK, Cherepanov P, Engelman AN. Nucleic Acids Res. 2019 May 21; 47(9):4663-4683.

RefSeq mRNA
See reference mRNA sequence for the Tnpo3 gene (XM_006236186.5).
RefSeq protein isoforms
See 4 reference sequence protein isoforms for the Tnpo3 gene.

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GlyGen glycoinformatics resource [GlyGen glycoinformatics resou...]
GlyGen glycoinformatics resource
reagents [ExactAntigen/Labome]
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