Thyrotoxic Periodic Paralysis Gene Set
Genes
14 genes associated with the disease Thyrotoxic Periodic Paralysis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
AAMDC
|
adipogenesis associated, Mth938 domain containing
|
|
ABCC8
|
ATP-binding cassette, sub-family C (CFTR/MRP), member 8
|
|
ADRB2
|
adrenoceptor beta 2, surface
|
|
ATP1B4
|
ATPase, Na+/K+ transporting, beta 4 polypeptide
|
|
CACNA1S
|
calcium channel, voltage-dependent, L type, alpha 1S subunit
|
|
DCHS2
|
dachsous cadherin-related 2
|
|
GABRA3
|
gamma-aminobutyric acid (GABA) A receptor, alpha 3
|
|
HLA-A
|
major histocompatibility complex, class I, A
|
|
HLA-DQA1
|
major histocompatibility complex, class II, DQ alpha 1
|
|
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
|
|
TNS3
|
tensin 3
|
