abnormality of chloride homeostasis Gene Set
Genes
14 genes associated with the abnormality of chloride homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
BSND
|
barttin CLCNK-type chloride channel accessory beta subunit
|
|
CFTR
|
cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
|
|
CLCNKA
|
chloride channel, voltage-sensitive Ka
|
|
CLCNKB
|
chloride channel, voltage-sensitive Kb
|
|
CUL3
|
cullin 3
|
|
FUCA1
|
fucosidase, alpha-L- 1, tissue
|
|
KCNJ1
|
potassium channel, inwardly rectifying subfamily J, member 1
|
|
KLHL3
|
kelch-like family member 3
|
|
SCNN1A
|
sodium channel, non voltage gated 1 alpha subunit
|
|
SCNN1B
|
sodium channel, non voltage gated 1 beta subunit
|
|
SLC12A1
|
solute carrier family 12 (sodium/potassium/chloride transporter), member 1
|
|
SLC26A3
|
solute carrier family 26 (anion exchanger), member 3
|
|
WNK1
|
WNK lysine deficient protein kinase 1
|
|
WNK4
|
WNK lysine deficient protein kinase 4
|
