KCNS3 - potassium voltage-gated channel modifier subfamily S member 3 Gene
Also Known as KV9.3
Species: Homo sapiens
About KCNS3
This gene has 5 transcripts (splice variants), 255 orthologues and 31 paralogues. Broad expression in lung (RPKM 12.4), placenta (RPKM 5.3) and 18 other tissues.
Summary
Voltage-gated potassium channels form the largest and most diversified class of ion channels and are present in both excitable and nonexcitable cells. Their main functions are associated with the regulation of the resting membrane potential and the control of the shape and frequency of action potentials. The alpha subunits are of 2 types: those that are functional by themselves and those that are electrically silent but capable of modulating the activity of specific functional alpha subunits. The protein encoded by this gene is not functional by itself but can form heteromultimers with member 1 and with member 2 (and possibly Other members) of the Shab-related subfamily of potassium voltage-gated channel proteins. This gene belongs to the S subfamily of the Potassium Channel family. Alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Sep 2013]
KCNS3 Products (2)
| mRNA | Protein | Name |
|---|---|---|
| NM_001282428.2 | NP_001269357.1 | potassium voltage-gated channel subfamily S member 3 |
| NM_002252.5 | NP_002243.3 | potassium voltage-gated channel subfamily S member 3 |
KCNS3 Protein Structure
BTB_2: BTB/POZ domain (17 - 116)
Ion_trans: Ion transport protein (225 - 405)
- 0
- 100
- 200
- 300
- 400
- 491 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
potassium voltage-gated channel subfamily S member 3 |
|
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Developmental And Epileptic Encephalopathy 52 |
|
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| Gallbladder Benign Neoplasm |
|