Scnn1b - sodium channel epithelial 1 subunit beta Gene
Also Known as RNENACB
Species: Rattus norvegicus
Summary
Enables WW domain binding activity and ligand-gated Sodium Channel activity. Contributes to sodium ion transmembrane transporter activity. Involved in several processes, including response to hypoxia; sodium ion transport; and wound healing, spreading of epidermal cells. Located in apical plasma membrane and cell surface. Used to study nephrotic syndrome. Human ortholog(s) of this gene implicated in Liddle syndrome; autosomal recessive pseudohypoaldosteronism type 1; bronchiectasis 1; and pseudohypoaldosteronism. Orthologous to human SCNN1B (Sodium Channel epithelial 1 subunit beta). [provided by Alliance of Genome Resources, Apr 2022]
Scnn1b Products (1)
| mRNA | Protein | Name |
|---|---|---|
| NM_012648.1 | NP_036780.1 | amiloride-sensitive sodium channel subunit beta |
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
amiloride-sensitive sodium channel subunit beta |
|
|
Related Agents
- Pre-clinical Phase
Pre-clinical Phase
| Cat. No. | Product Name |
Effect
|
Purity |
Rare Diseases
|
|---|---|---|---|---|
| HY-RS12553 | SCNN1B Human Pre-designed siRNA Set A | Pre-designed Set | / | Unkown |
Compound Screening Libraries
Virtual Screening
Customize Your Library
Drug Screening Service