Mus musculus eukaryotic translation elongation factor 1 alpha 2 (Eef1a - Nucleotide

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Face-valid phenotypes in a mouse model of the most common mutation in EEF1A2-related neurodevelopmental disorder. [Dis Model Mech. 2024]
Face-valid phenotypes in a mouse model of the most common mutation in EEF1A2-related neurodevelopmental disorder.
Marshall GF, Fasol M, Davies FCJ, Le Seelleur M, Fernandez Alvarez A, Bennett-Ness C, Gonzalez-Sulser A, Abbott CM. Dis Model Mech. 2024 Jun 1; 17(6). Epub 2024 Feb 2.
Autism- and epilepsy-associated EEF1A2 mutations lead to translational dysfunction and altered actin bundling. [Proc Natl Acad Sci U S A. 2023]
Autism- and epilepsy-associated EEF1A2 mutations lead to translational dysfunction and altered actin bundling.
Mohamed MS, Klann E. Proc Natl Acad Sci U S A. 2023 Sep 19; 120(38):e2307704120. Epub 2023 Sep 11.
Endogenous epitope tagging of eEF1A2 in mice reveals early embryonic expression of eEF1A2 and subcellular compartmentalisation of neuronal eEF1A1 and eEF1A2. [Mol Cell Neurosci. 2023]
Endogenous epitope tagging of eEF1A2 in mice reveals early embryonic expression of eEF1A2 and subcellular compartmentalisation of neuronal eEF1A1 and eEF1A2.
Davies FCJ, Marshall GF, Pegram E, Gadd D, Abbott CM. Mol Cell Neurosci. 2023 Sep; 126:103879. Epub 2023 Jul 8.

RefSeq protein product
See the reference protein sequence for elongation factor 1-alpha 2 (NP_031932.1).

Protein
Protein sequence from Nucleotide coding region
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Order EEF1A2 cDNA clone/Protein/Antibody/RNAi [OriGene]
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Nucleotide