GLRB FISH Probe

This gene encodes the beta subunit of the glycine receptor, which is a pentamer composed of alpha and beta subunits. The receptor functions as a neurotransmitter-gated ion channel, which produces hyperpolarization via increased chloride conductance due to the binding of glycine to the receptor. Mutations in this gene cause startle disease, also known as hereditary hyperekplexia or congenital stiff-person syndrome, a disease characterized by muscular rigidity. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]


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

Gene Summary

This gene encodes the beta subunit of the glycine receptor, which is a pentamer composed of alpha and beta subunits. The receptor functions as a neurotransmitter-gated ion channel, which produces hyperpolarization via increased chloride conductance due to the binding of glycine to the receptor. Mutations in this gene cause startle disease, also known as hereditary hyperekplexia or congenital stiff-person syndrome, a disease characterized by muscular rigidity. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]

Gene Details

Gene Symbol : GLRB

Gene Name : Glycine receptor beta

Chromosome : CHR 4: 157,076,124-157,172,089

Locus : 4q32.1

Alt. Genes : ZNF263

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