cytochrome c oxidase assembly protein COX20, mitochondrial isoform 3 [ - Protein

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Clinical and genetic characteristics of children with COX20-associated mitochondrial disorder: case report and literature review. [BMC Med Genomics. 2023]
Clinical and genetic characteristics of children with COX20-associated mitochondrial disorder: case report and literature review.
Chen L, Liu Y. BMC Med Genomics. 2023 Apr 24; 16(1):86. Epub 2023 Apr 24.
The phenotypic spectrum of COX20-associated mitochondrial disorder. [Brain. 2022]
The phenotypic spectrum of COX20-associated mitochondrial disorder.
Ban R, Kopajtich R, Lv J, Stenton SL, Shimura M, Wang Z, Yuan Y, Wang J, Han X, Liu Z, et al. Brain. 2022 Dec 19; 145(12):e125-e127.
Bi-allelic loss of function variants in COX20 gene cause autosomal recessive sensory neuronopathy. [Brain. 2021]
Bi-allelic loss of function variants in COX20 gene cause autosomal recessive sensory neuronopathy.
Dong HL, Ma Y, Yu H, Wei Q, Li JQ, Liu GL, Li HF, Chen L, Chen DF, Bai G, et al. Brain. 2021 Sep 4; 144(8):2457-2470.

RefSeq genomic sequence
See the genomic reference sequence for the COX20 gene (NG_042825.1).
RefSeq mRNA
See reference mRNA sequence for the COX20 gene (NM_001312873.1).
RefSeq protein isoforms
See 6 reference sequence protein isoforms for the COX20 gene.

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NOTCH antagonist SAHM1 effect on T-ALL cell lines
NOTCH antagonist SAHM1 effect on T-ALL cell lines
Accession: GDS3717

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