Homo sapiens hypothetical protein BC004337, mRNA (cDNA clone IMAGE:363 - 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.

Homo sapiens hypothetical protein BC004337, mRNA (cDNA clone IMAGE:3631943), par...
Homo sapiens hypothetical protein BC004337, mRNA (cDNA clone IMAGE:3631943), partial cds
gi|13279268|gb|BC004337.1|

Nucleotide
BX461213 Homo sapiens FETAL BRAIN Homo sapiens cDNA clone CS0DF024YA07 5-PRIME, ...
BX461213 Homo sapiens FETAL BRAIN Homo sapiens cDNA clone CS0DF024YA07 5-PRIME, mRNA sequence
gi|47055824|gnl|dbEST|22907439|emb| 213.2|

Nucleotide

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Nucleotide