This gene encodes a member of the protein arginine N-methyltransferase family of proteins. The encoded enzyme transfers single methyl groups to arginine residues to generate monomethylarginines on histone proteins as well as other protein substrates. This enzyme plays a role in a wide range of biological processes, including neuronal differentiation, male germ line imprinting, small nuclear ribonucleoprotein biogenesis, and regulation of the Wnt signaling pathway. Mutations in this gene underlie multiple related syndromes in human patients characterized by intellectual disability, short stature and other features. The encoded protein may promote breast cancer cell invasion and metastasis in human patients. [provided by RefSeq, May 2017]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| PRMT7-20-RE | 20 (40 μL) | 200 μL |  |
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| PRMT7-20-OR | 20 (40 μL) | 200 μL |  |
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| PRMT7-20-GO | 20 (40 μL) | 200 μL |  |
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| PRMT7-20-GR | 20 (40 μL) | 200 μL |  |
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| PRMT7-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a member of the protein arginine N-methyltransferase family of proteins. The encoded enzyme transfers single methyl groups to arginine residues to generate monomethylarginines on histone proteins as well as other protein substrates. This enzyme plays a role in a wide range of biological processes, including neuronal differentiation, male germ line imprinting, small nuclear ribonucleoprotein biogenesis, and regulation of the Wnt signaling pathway. Mutations in this gene underlie multiple related syndromes in human patients characterized by intellectual disability, short stature and other features. The encoded protein may promote breast cancer cell invasion and metastasis in human patients. [provided by RefSeq, May 2017]
Gene Symbol : PRMT7
Gene Name : Protein arginine methyltransferase 7
Chromosome : CHR 16: 683,109,73-683,588,31
Locus : 16q22.1
Alt. Genes : FEM1B
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