importin-8 isoform X1 [Homo sapiens]

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Bi-allelic variants in IPO8 cause a connective tissue disorder associated with cardiovascular defects, skeletal abnormalities, and immune dysregulation. [Am J Hum Genet. 2021]
Bi-allelic variants in IPO8 cause a connective tissue disorder associated with cardiovascular defects, skeletal abnormalities, and immune dysregulation.
Ziegler A, Duclaux-Loras R, Revenu C, Charbit-Henrion F, Begue B, Duroure K, Grimaud L, Guihot AL, Desquiret-Dumas V, Zarhrate M, et al. Am J Hum Genet. 2021 Jun 3; 108(6):1126-1137. Epub 2021 May 18.
Functional characterization of importin α8 as a classical nuclear localization signal receptor. [Biochim Biophys Acta. 2015]
Functional characterization of importin α8 as a classical nuclear localization signal receptor.
Kimoto C, Moriyama T, Tsujii A, Igarashi Y, Obuse C, Miyamoto Y, Oka M, Yoneda Y. Biochim Biophys Acta. 2015 Oct; 1853(10 Pt A):2676-83. Epub 2015 Jul 26.
Identification of importin 8 (IPO8) as the most accurate reference gene for the clinicopathological analysis of lung specimens. [BMC Mol Biol. 2008]
Identification of importin 8 (IPO8) as the most accurate reference gene for the clinicopathological analysis of lung specimens.
Nguewa PA, Agorreta J, Blanco D, Lozano MD, Gomez-Roman J, Sanchez BA, Valles I, Pajares MJ, Pio R, Rodriguez MJ, et al. BMC Mol Biol. 2008 Nov 17; 9:103. Epub 2008 Nov 17.

RefSeq mRNA
See reference mRNA sequence for the IPO8 gene (XM_017018691.3).
RefSeq protein isoforms
See 9 reference sequence protein isoforms for the IPO8 gene.

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Homo sapiens netrin 1 (NTN1), mRNA
Homo sapiens netrin 1 (NTN1), mRNA
gi|1519243046|ref|NM_004822.3|

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