PTCD3 protein, partial [Homo sapiens]

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Leigh syndrome is the main clinical characteristic of PTCD3 deficiency. [Brain Pathol. 2023]
Leigh syndrome is the main clinical characteristic of PTCD3 deficiency.
Muñoz-Pujol G, Ortigoza-Escobar JD, Paredes-Fuentes AJ, Jou C, Ugarteburu O, Gort L, Yubero D, García-Cazorla A, O'Callaghan M, Campistol J, et al. Brain Pathol. 2023 May; 33(3):e13134. Epub 2022 Nov 30.
PTCD3 mutations cause Leigh-like rather than Leigh syndrome. [Neurogenetics. 2019]
PTCD3 mutations cause Leigh-like rather than Leigh syndrome.
Finsterer J, Scorza CA, Scorza FA. Neurogenetics. 2019 Mar; 20(1):53-54. Epub 2019 Jan 31.
Mitochondrial ribosomal protein PTCD3 mutations cause oxidative phosphorylation defects with Leigh syndrome. [Neurogenetics. 2019]
Mitochondrial ribosomal protein PTCD3 mutations cause oxidative phosphorylation defects with Leigh syndrome.
Borna NN, Kishita Y, Kohda M, Lim SC, Shimura M, Wu Y, Mogushi K, Yatsuka Y, Harashima H, Hisatomi Y, et al. Neurogenetics. 2019 Mar; 20(1):9-25. Epub 2019 Jan 3.

RefSeq protein
See the reference protein sequence for small ribosomal subunit protein mS39 precursor (NP_060422.4).

Nucleotide
Nucleotide sequence from coding region
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Transcript/Protein Information [PANTHER Classification System]
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reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

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Protein