Entity Details
Primary name |
SLC6A2 |
Entity type |
gene |
Source |
Source Link |
Details
PrimaryID | 6530 |
RefseqGene | NG_016969 |
Symbol | SLC6A2 |
Name | solute carrier family 6 member 2 |
Chromosome | 16 |
Location | 16q12.2 |
TaxID | 9606 |
Status | live |
SourceGenome | genomic |
SourceOrigin | natural |
CreationDate | 1997-12-05 |
ModificationDate | 2021-06-13 |
Diseases
Show/Hide Table
Disease ID | Source | Name | Description |
604715 | OMIM | Orthostatic intolerance (OI) | Syndrome characterized by lightheadedness, fatigue, altered mentation and syncope. It is associated with postural tachycardia. Plasma norepinephrine concentration is abnormally high. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
5 interactions