GLRA1
This gene encodes a protein that functions as a subunit of a pentameric inhibitory glycine receptor, which controls postsynaptic inhibition in the brain. Startle disease (STHE), also known as hereditary hyperekplexia or congenital stiff-person syndrome, is caused by defects in this gene.
| Full Name | Glycine receptor alpha 1 |
| Gene ID | Human: 2741 Mouse: 14654 Rat: 25674 Monkey: 713940 |
| UniProt ID | Human: P23415 Mouse: Q64018 Rat: P07727 Monkey: F7GTN8 |
| Alternative Names | STHE; HKPX1; glycine receptor subunit alpha-1; glycine receptor 48 kDa subunit; glycine receptor strychnine-binding subunit; GLRA1; Glycine receptor alpha 1 |
Product List
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mProX™ Human GLRA1 Stable Cell Line
[CAT#: S01YF-1123-KX88]
- Product Category:
- Membrane Protein Stable Cell Lines
- Target Protein: GLRA1 Target Family: Voltage Gated Chloride Channel Target Protein Species: Human Host Cell Type: CHO-K1; HEK293
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