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This section gives an overview of the disease, and where available shows the following:
More information can be found in the help pages.
✖Disease ID: | 457 | |
Name: | Hyperkalemic Periodic Paralysis; HYPP | |
Associated with: | 1 target |
Database Links |
Disease Ontology:
DOID:14451 OMIM: 170500 Orphanet: ORPHA682 |
Click on the target name to link to its detailed view page
Where available, information is display on the role of the target in the disease; drugs which target the disease and their therapeutic use and side-effects.
If there is mutation data curated in GtoPdb this is indicated, with a link back to the appropriate section on the target detailed view page
Immuno ligand interactions - If available, a table of immuno-relevant ligands is shown. These ligands have been curated as having an association to the disease and possess interaction data with the target in GtoPdb. The approval status of the ligand is shown, along with curator comments and an indication of whether the target is considered the primary target of the ligand.
More information can be found in the help pages.
✖Nav1.4 | |
References: | 2-4 |
Mutations: | Nav1.4 is associated with 11 mutation. Click here for details ![]() |
Click ligand name to view ligand summary page
Click the arrow in the final column to expand comments
More information can be found in the help pages.
✖No ligand related data available for Hyperkalemic Periodic Paralysis; HYPP
1. Bendahhou S, Cummins TR, Kula RW, Fu YH, Ptácek LJ. (2002) Impairment of slow inactivation as a common mechanism for periodic paralysis in DIIS4-S5. Neurology, 58 (8): 1266-72. [PMID:11971097]
2. Cannon SC. (2002) An expanding view for the molecular basis of familial periodic paralysis. Neuromuscul Disord, 12 (6): 533-43. [PMID:12117476]
3. George AL. (2005) Inherited disorders of voltage-gated sodium channels. J Clin Invest, 115 (8): 1990-9. [PMID:16075039]
4. Lehmann-Horn F, Jurkat-Rott K. (1999) Voltage-gated ion channels and hereditary disease. Physiol Rev, 79 (4): 1317-72. [PMID:10508236]
5. Miller TM, Dias da Silva MR, Miller HA, Kwiecinski H, Mendell JR, Tawil R, McManis P, Griggs RC, Angelini C, Servidei S, Petajan J, Dalakas MC, Ranum LP, Fu YH, Ptácek LJ. (2004) Correlating phenotype and genotype in the periodic paralyses. Neurology, 63 (9): 1647-55. [PMID:15534250]
6. Ptácek LJ, George Jr AL, Griggs RC, Tawil R, Kallen RG, Barchi RL, Robertson M, Leppert MF. (1991) Identification of a mutation in the gene causing hyperkalemic periodic paralysis. Cell, 67 (5): 1021-7. [PMID:1659948]
7. Rojas CV, Wang JZ, Schwartz LS, Hoffman EP, Powell BR, Brown Jr RH. (1991) A Met-to-Val mutation in the skeletal muscle Na+ channel alpha-subunit in hyperkalaemic periodic paralysis. Nature, 354 (6352): 387-9. [PMID:1659668]
8. Wagner S, Lerche H, Mitrovic N, Heine R, George AL, Lehmann-Horn F. (1997) A novel sodium channel mutation causing a hyperkalemic paralytic and paramyotonic syndrome with variable clinical expressivity. Neurology, 49 (4): 1018-25. [PMID:9339683]