Your search for "glra1" returned 262 TaqMan® SNP Genotyping Assays
glycine receptor alpha 1
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]
GLRA1, GLYRA1, HKPX1, NMF11, OSCILLATOR, OT, SPASMODIC, SPD, STHE
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