Slc4a11 - solute carrier family 4, sodium bicarbonate transporter-like, member 11 Gene
Also Known as BTR1; NaBC1
Species: Mus musculus
Summary
Predicted to enable ion transmembrane transporter activity; protein dimerization activity; and water transmembrane transporter activity. Involved in fluid transport; ion homeostasis; and regulation of mesenchymal stem cell differentiation. Located in basolateral plasma membrane. Is expressed in metanephros and vomeronasal organ. Used to study congenital hereditary endothelial dystrophy of cornea. 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_001081162.1 | NP_001074631.1 | solute carrier family 4 member 11 |
| Biological Process GO Annotation | Evidence | References | Source |
|---|---|---|---|
| involved in fluid transport |
IMP
IMP: Inferred from mutant phenotype
|
20185830 | MGI |
| involved in monoatomic ion homeostasis |
IMP
IMP: Inferred from mutant phenotype
|
20185830 | MGI |
| involved in regulation of mesenchymal stem cell differentiation |
IMP
IMP: Inferred from mutant phenotype
|
33247189 | MGI |
| Cellular Component GO Annotation | Evidence | References | Source |
|---|---|---|---|
| located in basolateral plasma membrane |
IDA
IDA: Inferred from direct assay
|
23813972 | MGI |
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
solute carrier family 4 member 11 sodium bicarbonate transporter-like protein 11 |
|
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