hypokalemia Gene Set
Genes
9 gene mutations causing the hypokalemia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol |
Name |
|
ATP6V0A4
|
ATPase, H+ transporting, lysosomal V0 subunit a4
|
|
BSND
|
barttin CLCNK-type chloride channel accessory beta subunit
|
|
CYP11B1
|
cytochrome P450, family 11, subfamily B, polypeptide 1
|
|
CYP11B2
|
cytochrome P450, family 11, subfamily B, polypeptide 2
|
|
HNF4A
|
hepatocyte nuclear factor 4, alpha
|
|
LOC102723475
|
putative uncharacterized protein LOC388820
|
|
SCNN1B
|
sodium channel, non voltage gated 1 beta subunit
|
|
STK39
|
serine threonine kinase 39
|
|
WNK4
|
WNK lysine deficient protein kinase 4
|
