Periodic Hypokalemic Paresis Gene Set
Genes
9 genes associated with the disease Periodic Hypokalemic Paresis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
CA2
|
carbonic anhydrase II
|
|
CACNA1S
|
calcium channel, voltage-dependent, L type, alpha 1S subunit
|
|
CDH23
|
cadherin-related 23
|
|
GABRA3
|
gamma-aminobutyric acid (GABA) A receptor, alpha 3
|
|
KCNE3
|
potassium channel, voltage gated subfamily E regulatory beta subunit 3
|
|
KCNJ18
|
potassium channel, inwardly rectifying subfamily J, member 18
|
|
KCNJ2
|
potassium channel, inwardly rectifying subfamily J, member 2
|
|
SCN4A
|
sodium channel, voltage gated, type IV alpha subunit
|
|
SLC4A1
|
solute carrier family 4 (anion exchanger), member 1 (Diego blood group)
|
