KCNH2
A voltage-activated potassium channel component is encoded by this gene and is present in heart muscle, nerve cells, and microglia. A functional potassium channel is created when four copies of this protein collaborate with one copy of KCNE2. Long QT syndrome type 2 can be caused by mutations in this gene.
| Full Name | Potassium voltage-gated channel subfamily H member 2 |
| Gene ID | Human: 3757 Mouse: 16511 Rat: 117018 Monkey: 714174 |
| UniProt ID | Human: Q12809 Mouse: O35219 Rat: O08962 Monkey: F6WEE3 |
| Alternative Names | ERG1; HERG; LQT2; SQT1; ERG-1; H-ERG; HERG1; Kv11.1; potassium voltage-gated channel subfamily H member 2; eag homolog; eag-related protein 1; ether-a-go-go-related gene potassium channel 1; ether-a-go-go-related potassium channel protein; ether-a-go-go-related protein 1; human ether-a-go-go-related; long QT syndrome type 2; potassium channel, voltage gated eag related subfamily H, member 2; potassium voltage-gated channel, subfamily H (eag-related), member 2; voltage-gated potassium channel subunit Kv11.1; KCNH2; Potassium voltage-gated channel subfamily H member 2 |
Product List
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Magic™ mPro Human KCNH2 Cell Line
[CAT#: S01YF-1122-KX101]
- Product Category:
- Membrane Protein Stable Cell Lines
- Target Protein: KCNH2 Target Family: Voltage Gated Potassium Channel Target Protein Species: Human
mProX™ Human KCNH2 Stable Cell Line
[CAT#: S01YF-1123-KX35]
- Product Category:
- Membrane Protein Stable Cell Lines
- Target Protein: KCNH2 Target Family: Kv7 Target Protein Species: Human Host Cell Type: CHO-K1; HEK293
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