The protein encoded by this gene is a membrane protein that catalyzes the addition of an alkyl group from an akylamine to a glutamine residue of a protein, forming an alkylglutamine in the protein. This protein alkylation leads to crosslinking of proteins and catenation of polyamines to proteins. This gene contains either one or two copies of a 22 nt repeat unit in its 3' UTR. Mutations in this gene have been associated with autosomal recessive lamellar ichthyosis (LI) and nonbullous congenital ichthyosiform erythroderma (NCIE). [provided by RefSeq, Jul 2008]
SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
TGM1-20-RE | 20 (40 μL) | 200 μL | ![]() |
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TGM1-20-OR | 20 (40 μL) | 200 μL | ![]() |
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TGM1-20-GO | 20 (40 μL) | 200 μL | ![]() |
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TGM1-20-GR | 20 (40 μL) | 200 μL | ![]() |
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TGM1-20-AQ | 20 (40 μL) | 200 μL | ![]() |
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The protein encoded by this gene is a membrane protein that catalyzes the addition of an alkyl group from an akylamine to a glutamine residue of a protein, forming an alkylglutamine in the protein. This protein alkylation leads to crosslinking of proteins and catenation of polyamines to proteins. This gene contains either one or two copies of a 22 nt repeat unit in its 3' UTR. Mutations in this gene have been associated with autosomal recessive lamellar ichthyosis (LI) and nonbullous congenital ichthyosiform erythroderma (NCIE). [provided by RefSeq, Jul 2008]
Gene Symbol : TGM1
Gene Name : Transglutaminase 1
Chromosome : CHR 14: 242,632,09-242,491,13
Locus : 14q12
Alt. Genes : AKAP9
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