mitochondrial succinyl-CoA ligase [ADP-forming] subunit beta [Homo sap - Protein

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SUCLA2 Arg407Trp mutation can cause a nonprogressive movement disorder - deafness syndrome. [Ann Clin Transl Neurol. 2021]
SUCLA2 Arg407Trp mutation can cause a nonprogressive movement disorder - deafness syndrome.
Alkhater RA, Ahonen S, Minassian BA. Ann Clin Transl Neurol. 2021 Jan; 8(1):252-258. Epub 2020 Nov 24.
Co-occurring Down syndrome and SUCLA2-related mitochondrial depletion syndrome. [Am J Med Genet A. 2017]
Co-occurring Down syndrome and SUCLA2-related mitochondrial depletion syndrome.
Couser NL, Marchuk DS, Smith LD, Arreola A, Kaiser-Rogers KA, Muenzer J, Pandya A, Gucsavas-Calikoglu M, Powell CM. Am J Med Genet A. 2017 Oct; 173(10):2720-2724. Epub 2017 Jul 27.
Knockdown of Sucla2 decreases the viability of mouse spermatocytes by inducing apoptosis through injury of the mitochondrial function of cells. [Folia Histochem Cytobiol. 2016]
Knockdown of Sucla2 decreases the viability of mouse spermatocytes by inducing apoptosis through injury of the mitochondrial function of cells.
Huang S, Wang J, Wang L. Folia Histochem Cytobiol. 2016; 54(3):134-142.

RefSeq genomic sequence
See the genomic reference sequence for the SUCLA2 gene (NG_008241.2).
RefSeq protein
See the reference protein sequence for succinate--CoA ligase (NP_003841.1).

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mitochondrial succinyl-CoA ligase [ADP-forming] subunit beta [Homo sapiens]
mitochondrial succinyl-CoA ligase [ADP-forming] subunit beta [Homo sapiens]
gi|311349192|gb|ADP91761.1|

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