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SLC6A5
Solute carrier family 6 member 5GLYT2, NET1
This gene encodes a sodium- and chloride-dependent glycine neurotransmitter transporter. This integral membrane glycoprotein is responsible for the clearance of extracellular glycine during glycine-mediated neurotransmission. This protein is found in glycinergic axons and maintains a high presynaptic pool of neurotransmitter at glycinergic synapses. Mutations in this gene cause hyperekplexia; a heterogenous neurological disorder characterized by exaggerated startle responses and neonatal apnea. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2016]
Top validated antibodies |
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| antibodies-online |  ABIN2781602 |
Polyclonal |
WB
IHC
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| BioLegend | 870801 |
Monoclonal |
WB
ICC
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| Novus Biologicals | H00009152-M01 |
Monoclonal |
WB
EL
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| Invitrogen Antibodies | MA5-52662 |
Monoclonal |
WB
FC
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| Biorbyt | orb2120096 |
Polyclonal |
WB
IHC
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