Homo sapiens peroxisomal biogenesis factor 6 (PEX6), transcript varian - Nucleotide

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[Zellweger syndrome caused by PEX6 gene variation in 2 cases and literature review]. [Zhonghua Er Ke Za Zhi. 2024]
[Zellweger syndrome caused by PEX6 gene variation in 2 cases and literature review].
Yang P, Zeng CZ, Tao XW, Rong SW, Long Y, Zeng LK. Zhonghua Er Ke Za Zhi. 2024 Jan 2; 62(1):43-48.
A homozygous Gly470Ala variant in PEX6 causes severe Zellweger spectrum disorder. [Am J Med Genet A. 2023]
A homozygous Gly470Ala variant in PEX6 causes severe Zellweger spectrum disorder.
Galarreta CI, Wong K, Carmichael J, Woods J, Tise CG, Niehaus AD, Schildt AJ, Verscaj CP, Cusmano-Ozog KP. Am J Med Genet A. 2023 Aug; 191(8):2057-2063. Epub 2023 May 5.
A dual-activity topoisomerase complex regulates mRNA translation and turnover. [Nucleic Acids Res. 2022]
A dual-activity topoisomerase complex regulates mRNA translation and turnover.
Su S, Xue Y, Sharov A, Zhang Y, Lee SK, Martindale JL, Li W, Ku WL, Zhao K, De S, et al. Nucleic Acids Res. 2022 Jul 8; 50(12):7013-7033.

RefSeq protein product
See the reference protein sequence for peroxisome biogenesis factor 6 isoform 2 (NP_001303242.1).

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Nucleotide