Homo sapiens protein arginine methyltransferase 9 (PRMT9), RefSeqGene - Nucleotide

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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.
Arginine methylation of HSPA8 by PRMT9 inhibits ferroptosis to accelerate hepatitis B virus-associated hepatocellular carcinoma progression. [J Transl Med. 2023]
Arginine methylation of HSPA8 by PRMT9 inhibits ferroptosis to accelerate hepatitis B virus-associated hepatocellular carcinoma progression.
Deng W, Ai J, Zhang W, Zhou Z, Li M, Yan L, Zhang L, Huang Z, Wu Z, Ai J, et al. J Transl Med. 2023 Sep 15; 21(1):625. Epub 2023 Sep 15.
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.

RefSeq alternative splicing
See 10 reference mRNA sequence splice variants for the PRMT9 gene.

Protein
Protein sequence from Nucleotide coding region
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RNA
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Nucleotide