Details
| Type | Protein Coding |
| Official Symbol | SLC16A1 |
| Official Name | solute carrier family 16 member 1 [Source:HGNC Symbol;Acc:HGNC:10922] |
| Ensembl ID | ENSG00000281917 |
| Bio databases IDs | |
| Aliases | solute carrier family 16 member 1 |
| Species | Human, Homo sapiens |
Top Findings
The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
phenotypes
- ERYTHROCYTE LACTATE TRANSPORTER DEFECT
- HYPERINSULINEMIC HYPOGLYCEMIA FAMILIAL 7
- MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY