Symbol
| SLC9A3
| contributors: mct/pgu - updated : 11-10-2018
|
HGNC name
| solute carrier family 9 (sodium/hydrogen exchanger), isoform 3
|
HGNC id
| 11073
|
corresponding disease(s)
|
DIAR8
|
Other morbid association(s)
|
Type | Gene Modification | Chromosome rearrangement | Protein expression | Protein Function
|
---|
constitutional
|  
|  
| --over
|  
|
in Barrett esophagus  | tumoral
|  
| amplification
|  
|  
|
in early stages of non-small cell lung cancer | constitutional
|  
|  
| --low
|  
|
in patients with ulcerative colitis  | |
Susceptibility
|
to the sudden infant death syndrome (SIDS) to preeclampsia |
Variant & Polymorphism
other
| the level of SLC9A3 expression in brainstem tissue may contribute to the vulnerability of infants for SIDS |
|
Rs4957061 in SLC9A3 was significantly associated with a reduced risk of preeclampsia in whites |
|
|
Candidate gene
Marker
Therapy target
| | | |
| depleted Slc9a3 in male mice causes infertility due to the abnormal dilated lumen of the rete testis and efferent ductules  | |
Cftr expression was dramatically decreased in the epididymis and vas deferens of Slc9a3 knockout mice  |