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1 records found for search term Glra1
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RGD IDSymbolNameDescriptionChrStartStopSpeciesAnnotationsMatchType
730939GLRA1glycine receptor alpha 1The 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. Mul5151822513151924851Human341symbol , COSMIC , Human Proteome Mapgene, protein-coding, REVIEWED [RefSeq]