POMGNT1 FISH Probe

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 Details
SKU Test Kits Buffer Dye Color Order Now
POMGNT1-20-RE 20 (40 μL) 200 μL color Request Pricing
POMGNT1-20-OR 20 (40 μL) 200 μL color Request Pricing
POMGNT1-20-GO 20 (40 μL) 200 μL color Request Pricing
POMGNT1-20-GR 20 (40 μL) 200 μL color Request Pricing
POMGNT1-20-AQ 20 (40 μL) 200 μL color Request Pricing

Gene Summary

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 Details

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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