Homo sapiens proline rich transmembrane protein 2 (PRRT2), transcript - Nucleotide

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Effects of PRRT2 mutation on brain gray matter networks in paroxysmal kinesigenic dyskinesia. [Cereb Cortex. 2024]
Effects of PRRT2 mutation on brain gray matter networks in paroxysmal kinesigenic dyskinesia.
Li X, Lei D, Qin K, Li L, Zhang Y, Zhou D, Kemp GJ, Gong Q. Cereb Cortex. 2024 Jan 14; 34(1).
Missense mutations in the membrane domain of PRRT2 affect its interaction with Nav1.2 voltage-gated sodium channels. [Neurobiol Dis. 2023]
Missense mutations in the membrane domain of PRRT2 affect its interaction with Nav1.2 voltage-gated sodium channels.
Sterlini B, Franchi F, Morinelli L, Corradi B, Parodi C, Albini M, Bianchi A, Marte A, Baldelli P, Alberini G, et al. Neurobiol Dis. 2023 Jul; 183:106177. Epub 2023 Jun 2.
Peri-ictal EEG in infants with PRRT2-related self-limited infantile epilepsy. [Epileptic Disord. 2023]
Peri-ictal EEG in infants with PRRT2-related self-limited infantile epilepsy.
Fearn N, Macdonald-Laurs E, Moylan L, Howell KB. Epileptic Disord. 2023 Aug; 25(4):510-518. Epub 2023 May 17.

RefSeq alternative splicing
See 11 reference mRNA sequence splice variants for the PRRT2 gene.
RefSeq protein product
See the reference protein sequence for proline-rich transmembrane protein 2 isoform 3 (NP_001243372.1).

Protein
Protein sequence from Nucleotide coding region
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Nucleotide