| GENE NAME | SLC9A6 |
| CHROMOSOME | X |
| ENSEMBL ID | ENSG00000198689 |
| ENTREZ ID | 10479 |
| UNIPROT ACCESSION NUMBER | Q92581 |
| GO MOLECULAR FUNCTION | antiporter activity; sodium:proton antiporter activity; solute:proton antiporter activity; potassium:proton antiporter activity |
| ESSENTIAL IN MOUSE | Non-essential |
| PATHWAYS | R-HSA-382551; R-HSA-5619092; R-HSA-1643685; R-HSA-425407; hsa04260; R-HSA-5619115; hsa04260; R-HSA-5619115; R-HSA-1643685; R-HSA-425407; R-HSA-425393; R-HSA-5619092; R-HSA-382551; R-HSA-425986; R-HSA-5619102; R-HSA-425986; R-HSA-5619102; R-HSA-425393 |
| 1 combination linked to SLC9A6 | OLI432 |
| 1 variant linked to SLC9A6 | SLC9A6:c.1777C>G, p.Leu593Val |
| 1 disease linked to SLC9A6 | Rare pervasive developmental disorder |