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Details of SLC2A9 gene in Homo sapiens
IDs |
|---|
| Link outs |
Gene Name |
Alias |
Uniprot ID |
SwissProt ID |
NCBI gene ID |
ENSEMBL ID |
Description |
Source |
|
| SLC2A9 | GLUT9 | Q9NRM0 | GTR9_HUMAN | 56606
| ENSG00000109667
| Solute carrier family 2, facilitated glucose transporter member 9 | SPROT |
Disease |
|---|
| Disease |
OMIM id |
| Hypouricemia renal 2 (RHUC2) [MIM:612076]: A disorder characterized by impaired uric acid reabsorption at the apical membrane of proximal renal tubule cells, and high urinary urate excretion. Patients often appear asymptomatic, but may be subject to exercise-induced acute renal failure, chronic renal dysfunction and nephrolithiasis. Note=The disease is caused by mutations affecting the gene represented in this entry. |
612076 |
Orthologs in other species |
|---|
| M. musculus |
D. melonogaster |
C. elegans |
S. purpuratus |
| Slc2a9 | --- | --- | |
