| Protein Name | prestin |
|---|---|
| Organism | Drosophila melanogaster |
| Gene ID | 39996 |
| Gene Symbol | Prestin |
| UniProt | Q9VVM6 (Q9VVM6_DROME) |
| Relationships |
Total Number of functionally related compound(s) :
7
Total Number of Articles : 3 |
Description |
prestin |
| Gene Summary |
Enables calcium ion transmembrane transporter activity; inorganic anion transmembrane transporter activity; and organic anion transmembrane transporter activity. Involved in bicarbonate transport; carboxylic acid transport; and inorganic ion transmembrane transport. Predicted to be located in membrane. Predicted to be active in plasma membrane. Is expressed in adult head. Human ortholog(s) of this gene implicated in several diseases, including Pendred Syndrome; autosomal recessive nonsyndromic deafness (multiple); bone disease (multiple); calcium oxalate nephrolithiasis; and diarrhea (multiple). Orthologous to several human genes including SLC26A4 (solute carrier family 26 member 4); SLC26A5 (solute carrier family 26 member 5); and SLC26A6 (solute carrier family 26 member 6). [provided by Alliance of Genome Resources, Jul 2025] |
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| Properties | |