Homo sapiens aldehyde dehydrogenase 5 family member A1 (ALDH5A1), tran - Nucleotide

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Functional Characterization of a Spectrum of Genetic Variants in a Family with Succinic Semialdehyde Dehydrogenase Deficiency. [Int J Mol Sci. 2024]
Functional Characterization of a Spectrum of Genetic Variants in a Family with Succinic Semialdehyde Dehydrogenase Deficiency.
Didiasova M, Cesaro S, Feldhoff S, Bettin I, Tiegel N, Füssgen V, Bertoldi M, Tikkanen R. Int J Mol Sci. 2024 May 11; 25(10). Epub 2024 May 11.
Clinical and molecular outcomes from the 5-Year natural history study of SSADH Deficiency, a model metabolic neurodevelopmental disorder. [J Neurodev Disord. 2024]
Clinical and molecular outcomes from the 5-Year natural history study of SSADH Deficiency, a model metabolic neurodevelopmental disorder.
Tokatly Latzer I, Roullet JB, Afshar-Saber W, Lee HHC, Bertoldi M, McGinty GE, DiBacco ML, Arning E, Tsuboyama M, Rotenberg A, et al. J Neurodev Disord. 2024 Apr 24; 16(1):21. Epub 2024 Apr 24.
Interaction network of human early embryonic transcription factors. [EMBO Rep. 2024]
Interaction network of human early embryonic transcription factors.
Gawriyski L, Tan Z, Liu X, Chowdhury I, Malaymar Pinar D, Zhang Q, Weltner J, Jouhilahti EM, Wei GH, Kere J, et al. EMBO Rep. 2024 Mar; 25(3):1589-1622. Epub 2024 Jan 31.

RefSeq alternative splicing
See 3 reference mRNA sequence splice variants for the ALDH5A1 gene.
RefSeq protein product
See the reference protein sequence for succinate-semialdehyde dehydrogenase, mitochondrial isoform 3 (NP_001355883.1).

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Protein sequence from Nucleotide coding region
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Nucleotide