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familial hemiplegic migraine 2

Summary
Synonym
  • FHM2
  • Familial hemiplegic migraine-2
  • MHP2
Definition
A familial hemiplegic migraine that has_material_basis_in heterozygous mutation in ATP1A2 on 1q23.2.
Super Class
familial hemiplegic migraine
Disease Ontology
DOID:0111182
Mondo Disease Ontology
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
477 ATP1A2 ATPase Na+/K+ transporting subunit alpha 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
98660 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide
Displaying 1 entry
Gene ID Gene Symbol Description Source
24212 Atp1a2 ATPase Na+/K+ transporting subunit alpha 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
48971 Atpalpha Na pump alpha subunit
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International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: December 9, 2024