KCNJ2
Most mammalian cells include potassium channels, which are involved in a variety of physiologic reactions. This gene produces an inward-rectifier type potassium channel that is an integral membrane protein. The encoded protein likely plays a role in determining the action potential waveform and excitability of neuronal and muscular tissues because it has a stronger propensity to allow potassium to flow into cells as opposed to out of them. Andersen syndrome, which is characterized by recurrent paralysis, cardiac arrhythmias, and dysmorphic traits, has been linked to mutations in this gene.
| Full Name | Potassium inwardly rectifying channel subfamily J member 2 |
| Gene ID | Human: 3759 Mouse: 16518 Rat: 29712 Monkey: 574189 |
| UniProt ID | Human: P63252 Mouse: P35561 Rat: Q64273 Monkey: P63253 |
| Alternative Names | IRK1; LQT7; SQT3; ATFB9; HHIRK1; KIR2.1; HHBIRK1; inward rectifier potassium channel 2; IRK-1; cardiac inward rectifier potassium channel; hIRK1; inward rectifier K+ channel KIR2.1; potassium channel, inwardly rectifying subfamily J, member 2; potassium voltage-gated channel subfamily J member 2; KCNJ2; Potassium inwardly rectifying channel subfamily J member 2 |
Product List
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Magic™ mPro Human KCNJ2 Cell Line
[CAT#: S01YF-1122-KX93]
- Product Category:
- Membrane Protein Stable Cell Lines
- Target Protein: KCNJ2 Target Family: Potassium, Inward Rectifier Target Protein Species: Human
mProX™ Human KCNJ2 Stable Cell Line
[CAT#: S01YF-1123-KX42]
- Product Category:
- Membrane Protein Stable Cell Lines
- Target Protein: KCNJ2 Target Family: GIRK Target Protein Species: Human Host Cell Type: SCLC H69; H446; CHO-K1; HEK293
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