Varaico: Literature-Extracted Genetic Variants

Gene:PRMT6
Variant:p.D88A
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PRMT6

NM_018137.3:p.D88A

Associated Papers

Huntingtin-mediated axonal transport requires arginine methylation by PRMT6.

Migazzi A et al.

Cell Reports, 2021

A First-in-Class, Highly Selective and Cell-Active Allosteric Inhibitor of Protein Arginine Methyltransferase 6.

Shen Y et al.

Journal of Medicinal Chemistry, 2021

Skeletal muscle-specific Prmt1 deletion causes muscle atrophy via deregulation of the PRMT6-FOXO3 axis.

Choi S et al.

Autophagy, 2019

A Potent, Selective, and Cell-Active Inhibitor of Human Type I Protein Arginine Methyltransferases.

Eram MS et al.

Acs Chemical Biology, 2016

Protein arginine methyltransferase 6 enhances polyglutamine-expanded androgen receptor function and toxicity in spinal and bulbar muscular atrophy.

Scaramuzzino C et al.

Neuron, 2015

Automethylation of protein arginine methyltransferase 6 (PRMT6) regulates its stability and its anti-HIV-1 activity.

Singhroy DN et al.

Retrovirology, 2013

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."