The protein encoded by this gene is a subunit of a pentameric inhibitory glycine receptor, which mediates postsynaptic inhibition in the central nervous system. Defects in this gene are a cause of startle disease (STHE), also known as hereditary hyperekplexia or congenital stiff-person syndrome. Multiple transcript variants encoding different isoforms have been found. [provided by RefSeq, Dec 2015]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| GLRA1BA-20-REGO | 20 (40 μL) | 200 μL |
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| GLRA1BA-20-REGR | 20 (40 μL) | 200 μL |
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| GLRA1BA-20-ORGR | 20 (40 μL) | 200 μL |
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| GLRA1BA-20-GOGR | 20 (40 μL) | 200 μL |
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| GLRA1BA-20-GRRE | 20 (40 μL) | 200 μL |
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| GLRA1BA-20-GROR | 20 (40 μL) | 200 μL |
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| GLRA1BA-20-GRGO | 20 (40 μL) | 200 μL |
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| GLRA1BA-20-AQOR | 20 (40 μL) | 200 μL |
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The protein encoded by this gene is a subunit of a pentameric inhibitory glycine receptor, which mediates postsynaptic inhibition in the central nervous system. Defects in this gene are a cause of startle disease (STHE), also known as hereditary hyperekplexia or congenital stiff-person syndrome. Multiple transcript variants encoding different isoforms have been found. [provided by RefSeq, Dec 2015]
Gene Symbol : GLRA1
Gene Name : Glycine receptor alpha 1
Chromosome : CHR 5: 151,924,835-151,820,797
Locus : 5q33.1
Alt. Genes : ENAM
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