Mus musculus methylmalonyl-Coenzyme A mutase (Mmut), mRNA; nuclear gen - Nucleotide

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Maternal Ezh1/2 deficiency impairs the function of mitochondria in mouse oocytes and early embryos. [J Cell Physiol. 2024]
Maternal Ezh1/2 deficiency impairs the function of mitochondria in mouse oocytes and early embryos.
Zhang D, Deng W, Jiang T, Zhao Y, Bai D, Tian Y, Kong S, Zhang L, Wang H, Gao S, et al. J Cell Physiol. 2024 Jun; 239(6):e31244. Epub 2024 Mar 26.
Integrated multi-omics reveals anaplerotic rewiring in methylmalonyl-CoA mutase deficiency. [Nat Metab. 2023]
Integrated multi-omics reveals anaplerotic rewiring in methylmalonyl-CoA mutase deficiency.
Forny P, Bonilla X, Lamparter D, Shao W, Plessl T, Frei C, Bingisser A, Goetze S, van Drogen A, Harshman K, et al. Nat Metab. 2023 Jan; 5(1):80-95. Epub 2023 Jan 26.
Growth advantage of corrected hepatocytes in a juvenile model of methylmalonic acidemia following liver directed adeno-associated viral mediated nuclease-free genome editing. [Mol Genet Metab. 2022]
Growth advantage of corrected hepatocytes in a juvenile model of methylmalonic acidemia following liver directed adeno-associated viral mediated nuclease-free genome editing.
Venturoni LE, Chandler RJ, Liao J, Hoffmann V, Ramesh N, Gordo S, Chau N, Venditti CP. Mol Genet Metab. 2022 Sep-Oct; 137(1-2):1-8. Epub 2022 Jul 4.

RefSeq alternative splicing
See the other reference mRNA sequence splice variant for the Mmut gene (XM_017317291.3).
RefSeq protein product
See the reference protein sequence for methylmalonyl-CoA mutase, mitochondrial precursor (NP_032676.2).

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Nucleotide