G2Cdb::Human Disease report

Disease id
Thyrotoxic periodic paralysis
Nervous system disease

Genes (1)

Gene Name/Description Mutations Found Literature Mutations Type Genetic association?
G00001324 ATP1A1
ATPase, Na+/K+ transporting, alpha 1 polypeptide
Y (15001631) Single nucleotide polymorphism (SNP) N


Literature (1)

Pubmed - human_disease

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EUROSPIN (FP7-HEALTH-241498), SynSys (FP7-HEALTH-242167) and GENCODYS (FP7-HEALTH-241995).

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