Homo sapiens peroxisomal biogenesis factor 6 (PEX6), RefSeqGene on chr - 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.
ERVK13-1/miR-873-5p/GNMT Axis Promotes Metastatic Potential in Human Bladder Cancer though Sarcosine Production. [Int J Mol Sci. 2023]
ERVK13-1/miR-873-5p/GNMT Axis Promotes Metastatic Potential in Human Bladder Cancer though Sarcosine Production.
Kishi S, Mori S, Fujiwara-Tani R, Ogata R, Sasaki R, Ikemoto A, Goto K, Sasaki T, Miyake M, Sasagawa S, et al. Int J Mol Sci. 2023 Nov 15; 24(22). Epub 2023 Nov 15.
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.

RefSeq alternative splicing
See 8 reference mRNA sequence splice variants for the PEX6 gene.

Protein
Protein sequence from Nucleotide coding region
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Nucleotide