Kir2.1
- 1 min read
- 3 chapters
Explore on Lably
ToursExplore Lably’s 3D toursClinical significance
A defect in this gene is associated with Andersen-Tawil syndrome.
A mutation in the KCNJ2 gene has also been shown to cause short QT syndrome.
Sign in to keep reading
2 more chapters are free with a Lably account.
In research
In neurogenetics, Kir2.1 is used in Drosophila research to inhibit neurons, as overexpression of this channel will hyperpolarize cells.
In optogenetics, a trafficking sequence from Kir2.1 has been added to halorhodopsin to improve its membrane localization. The resulting protein eNpHR3.0 is used in optogenetic research to inhibit neurons with light.
Expression of Kir2.1 gene in human HEK293 cells induce a transient outward current, creating a steady membrane potential close to the reversal potential of potassium.
Interactions
Kir2.1 has been shown to interact with:
- DLG4,
- Interleukin 16, and
- TRAK2