Slc4a11 - solute carrier family 4 member 11 Gene
Species: Rattus norvegicus
Summary
Predicted to enable ion transmembrane transporter activity; protein dimerization activity; and water transmembrane transporter activity. Predicted to be involved in several processes, including anion transport; cation transport; and cellular hypotonic response. Located in basolateral plasma membrane and vesicle membrane. Human ortholog(s) of this gene implicated in Fuchs' endothelial dystrophy; congenital hereditary endothelial dystrophy of cornea; and corneal dystrophy-perceptive deafness syndrome. Orthologous to human SLC4A11 (solute carrier family 4 member 11). [provided by Alliance of Genome Resources, Apr 2022]
Slc4a11 Products (1)
| mRNA | Protein | Name |
|---|---|---|
| NM_001107775.1 | NP_001101245.1 | sodium bicarbonate transporter-like protein 11 |
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
sodium bicarbonate transporter-like protein 11 |
|
Related Agents
- Pre-clinical Phase
Pre-clinical Phase
| Cat. No. | Product Name |
Effect
|
Purity |
Rare Diseases
|
|---|---|---|---|---|
| HY-177554 | KB05yne | 99.97% | Unkown | |
| HY-185414 | KB05-Biotin | / | Unkown | |
| HY-RS13267 | SLC4A11 Human Pre-designed siRNA Set A | Pre-designed Set | / | Unkown |
Compound Screening Libraries
Virtual Screening
Customize Your Library
Drug Screening Service