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 |
Pathways
Biological processes and signaling networks where the SLC16A1 gene in human plays a role, providing insight into its function and relevance in health or disease.
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