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GLRA1

Official Full Name
glycine receptor alpha 1
Organism
Homo sapiens
GeneID
2741
Background
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]
Synonyms
STHE; HKPX1;

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