familial hemiplegic migraine 2 Disease Ontology Browser

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Disease Ontology Browser

familial hemiplegic migraine 2 (DOID:0111182)
Alliance: disease page
Synonyms: Familial hemiplegic migraine-2; FHM2; MHP2
Alt IDs: OMIM:602481
Definition: A familial hemiplegic migraine that has_material_basis_in heterozygous mutation in ATP1A2 on 1q23.2.

Disease References using Mouse Models (4)

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/23/2024 MGI 6.23

Allelic Composition	Genetic Background	Reference	Phenotypes
Atp1a2tm1.1Tmklh/Atp1a2+	B6.129S1(Cg)-Atp1a2^tm1.1Tmklh	J:259556	View
Atp1a2tm1.1Gica/Atp1a2+	B6.Cg-Atp1a2^tm1.1Gica	J:307518	View