This gene encodes a type II transmembrane protein that resides in the Golgi apparatus. It participates in O-mannosyl glycosylation and is specific for alpha linked terminal mannose. Mutations in this gene may be associated with muscle-eye-brain disease and several congenital muscular dystrophies. Alternatively spliced transcript variants that encode different protein isoforms have been described. [provided by RefSeq, Feb 2014]
SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
POMGNT1-20-RE | 20 (40 μL) | 200 μL | Request Pricing | |
POMGNT1-20-OR | 20 (40 μL) | 200 μL | Request Pricing | |
POMGNT1-20-GO | 20 (40 μL) | 200 μL | Request Pricing | |
POMGNT1-20-GR | 20 (40 μL) | 200 μL | Request Pricing | |
POMGNT1-20-AQ | 20 (40 μL) | 200 μL | Request Pricing |
This gene encodes a type II transmembrane protein that resides in the Golgi apparatus. It participates in O-mannosyl glycosylation and is specific for alpha linked terminal mannose. Mutations in this gene may be associated with muscle-eye-brain disease and several congenital muscular dystrophies. Alternatively spliced transcript variants that encode different protein isoforms have been described. [provided by RefSeq, Feb 2014]
Gene Symbol : POMGNT1
Gene Name : Protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)
Chromosome : CHR 1: 462,203,04-461,886,80
Locus : 1p34.1
Alt. Genes : ZNF263
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