periodic paralysis Gene Set
Genes
6 genes associated with the periodic paralysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
CA2
|
carbonic anhydrase II
|
|
CACNA1S
|
calcium channel, voltage-dependent, L type, alpha 1S subunit
|
|
FAH
|
fumarylacetoacetate hydrolase (fumarylacetoacetase)
|
|
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)
|
