protein arginine N-methyltransferase 9 isoform X1 [Mus musculus]

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Loss-of-function mutation in PRMT9 causes abnormal synapse development by dysregulation of RNA alternative splicing. [Nat Commun. 2024]
Loss-of-function mutation in PRMT9 causes abnormal synapse development by dysregulation of RNA alternative splicing.
Shen L, Ma X, Wang Y, Wang Z, Zhang Y, Pham HQH, Tao X, Cui Y, Wei J, Lin D, et al. Nat Commun. 2024 Apr 1; 15(1):2809. Epub 2024 Apr 1.
The protein arginine methyltransferase PRMT9 attenuates MAVS activation through arginine methylation. [Nat Commun. 2022]
The protein arginine methyltransferase PRMT9 attenuates MAVS activation through arginine methylation.
Bai X, Sui C, Liu F, Chen T, Zhang L, Zheng Y, Liu B, Gao C. Nat Commun. 2022 Aug 26; 13(1):5016. Epub 2022 Aug 26.
Genetic determinants of micronucleus formation in vivo. [Nature. 2024]
Genetic determinants of micronucleus formation in vivo.
Adams DJ, Barlas B, McIntyre RE, Salguero I, van der Weyden L, Barros A, Vicente JR, Karimpour N, Haider A, Ranzani M, et al. Nature. 2024 Mar; 627(8002):130-136. Epub 2024 Feb 14.

RefSeq mRNA
See reference mRNA sequence for the Prmt9 gene (XM_036153707.1).
RefSeq protein isoforms
See 4 reference sequence protein isoforms for the Prmt9 gene.

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Protein