
Gene Report
| Approved Symbol | SLC16A2 |
|---|---|
| Approved Name | solute carrier family 16, member 2 (thyroid hormone transporter) |
| Previous Symbol | DXS128, AHDS, MRX22 |
| Previous Name | solute carrier family 16 (monocarboxylic acid transporters), member 2 (putative transporter), "Allan-Herndon-Dudley syndrome", "solute carrier family 16 (monocarboxylic acid transporters), member 2", "mental retardation, X-linked 22", "solute carrier family 16, member 2 (monocarboxylic acid transporter 8)" |
| Symbol Alias | XPCT, MCT8, MCT7 |
| Location | Xq13.2 |
| Position | chrX:73641328-73753764 (+) |
| External Links |
Entrez Gene: 6567 Ensembl: ENSG00000147100 UCSC: uc004ebt.2 HGNC ID: 10923 |
| No. of Studies (Positive/Negative) | 1(1/0)
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| Type | Literature-origin |
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Note:
1. The different color of the nodes denotes the level of the nodes.
| Genetic/Epigenetic Locus | Protein and Other Molecule | Cell and Molecular Pathway | Neural System | Cognition and Behavior | Symptoms and Signs | Environment | MDD |
2. User can drag the nodes to rearrange the layout of the network. Click the node will enter the report page of the node. Right-click will show also the menus to link to the report page of the node and remove the node and related edges. Hover the node will show the level of the node and hover the edge will show the evidence/description of the edge.
3. The network is generated using Cytoscape Web
SLC16A2 related interactors from protein-protein interaction data in HPRD (count: 2)
