Periodic Paralysis (Finding) Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C1279412
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Genes

17 genes associated with the disease Periodic Paralysis (Finding) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ABCB6 ATP-binding cassette, sub-family B (MDR/TAP), member 6 (Langereis blood group)
CACNA1S calcium channel, voltage-dependent, L type, alpha 1S subunit
COL4A5 collagen, type IV, alpha 5
FAH fumarylacetoacetate hydrolase (fumarylacetoacetase)
HLA-B major histocompatibility complex, class I, B
KCNE3 potassium channel, voltage gated subfamily E regulatory beta subunit 3
KCNH2 potassium channel, voltage gated eag related subfamily H, member 2
KCNJ18 potassium channel, inwardly rectifying subfamily J, member 18
KCNJ2 potassium channel, inwardly rectifying subfamily J, member 2
MCM3AP minichromosome maintenance complex component 3 associated protein
PRKAA1 protein kinase, AMP-activated, alpha 1 catalytic subunit
PRKAA2 protein kinase, AMP-activated, alpha 2 catalytic subunit
PRKAB1 protein kinase, AMP-activated, beta 1 non-catalytic subunit
RYR1 ryanodine receptor 1 (skeletal)
SCN4A sodium channel, voltage gated, type IV alpha subunit
SLC4A1 solute carrier family 4 (anion exchanger), member 1 (Diego blood group)
TBC1D24 TBC1 domain family, member 24