Homo sapiens NMDAR1 subunit isoform 3b (hNMDAR1-3b) mRNA, complete cds

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De novo GRIN variants in M3 helix associated with neurological disorders control channel gating of NMDA receptor. [Cell Mol Life Sci. 2024]
De novo GRIN variants in M3 helix associated with neurological disorders control channel gating of NMDA receptor.
Xu Y, Song R, Perszyk RE, Chen W, Kim S, Park KL, Allen JP, Nocilla KA, Zhang J, XiangWei W, et al. Cell Mol Life Sci. 2024 Mar 28; 81(1):153. Epub 2024 Mar 28.
GRIN1 variants associated with neurodevelopmental disorders reveal channel gating pathomechanisms. [Epilepsia. 2023]
GRIN1 variants associated with neurodevelopmental disorders reveal channel gating pathomechanisms.
Ragnarsson L, Zhang Z, Das SS, Tran P, Andersson Å, des Portes V, Desmettre Altuzarra C, Remerand G, Labalme A, Chatron N, et al. Epilepsia. 2023 Dec; 64(12):3377-3388. Epub 2023 Oct 17.
Pluripotential GluN1 (NMDA NR1): Functional Significance in Cellular Nuclei in Pain/Nociception. [Int J Mol Sci. 2023]
Pluripotential GluN1 (NMDA NR1): Functional Significance in Cellular Nuclei in Pain/Nociception.
McNearney TA, Westlund KN. Int J Mol Sci. 2023 Aug 25; 24(17). Epub 2023 Aug 25.

RefSeq alternative splicing
See 13 reference mRNA sequence splice variants for the GRIN1 gene.

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Nucleotide