persulfide dioxygenase ETHE1, mitochondrial isoform 3 [Homo sapiens]

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Ethylmalonic encephalopathy ETHE1 p. D165H mutation alters the mitochondrial function in human skeletal muscle proteome. [Mitochondrion. 2021]
Ethylmalonic encephalopathy ETHE1 p. D165H mutation alters the mitochondrial function in human skeletal muscle proteome.
Sathe G, Deepha S, Gayathri N, Nagappa M, Parayil Sankaran B, Taly AB, Khanna T, Pandey A, Govindaraj P. Mitochondrion. 2021 May; 58:64-71. Epub 2021 Feb 24.
Ethylmalonic encephalopathy 1 initiates overactive autophagy in depleted uranium-induced cytotoxicity in the human embryonic kidney 293 cells. [J Biochem Mol Toxicol. 2021]
Ethylmalonic encephalopathy 1 initiates overactive autophagy in depleted uranium-induced cytotoxicity in the human embryonic kidney 293 cells.
Hao Y, Huang J, Ran Y, Wang S, Li J, Zhao Y, Ran X, Lu B, Liu J, Li R. J Biochem Mol Toxicol. 2021 Mar; 35(3):e22669. Epub 2020 Dec 4.
Deficiency of the mitochondrial sulfide regulator ETHE1 disturbs cell growth, glutathione level and causes proteome alterations outside mitochondria. [Biochim Biophys Acta Mol Basis...]
Deficiency of the mitochondrial sulfide regulator ETHE1 disturbs cell growth, glutathione level and causes proteome alterations outside mitochondria.
Sahebekhtiari N, Fernandez-Guerra P, Nochi Z, Carlsen J, Bross P, Palmfeldt J. Biochim Biophys Acta Mol Basis Dis. 2019 Jan; 1865(1):126-135. Epub 2018 Nov 2.

RefSeq genomic sequence
See the genomic reference sequence for the ETHE1 gene (NG_008141.1).
RefSeq mRNA
See reference mRNA sequence for the ETHE1 gene (NM_001320868.2).

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