About   Help   FAQ
Human Disease and Mouse Model Detail
Human Disease

Term: Migraine, Familial Hemiplegic, 1; FHM1
OMIM ID: 141500

Synonyms FHM
Associated Genes

Orthologous mouse and human markers where mutations in one or both species have been associated with phenotypes characteristic of this disease.

Mouse Gene
Human Gene
 
Characteristics of this human disease are associated with mutations in...
Cacna1a CACNA1A
  mousehuman...both mouse and human orthologous genes.
     

Mouse Models
Genotype Ref(s)
Allelic Composition Note Genetic Background
Models with phenotypic similarity to human disease where etiologies involve orthologs.1
Cacna1atm1Maag/Cacna1atm1Maag   involves: 129P2/OlaHsd * C57BL/6J J:88693
Cacna1atm1Maag/Cacna1atm1Maag   B6.129P2-Cacna1atm1Maag J:144701
Cacna1atm3Maag/Cacna1atm3Maag   B6.129P2-Cacna1atm3Maag J:144701

1Human genes are associated with this disease. Mouse model genotypes include mutations in the orthologs of these human genes.
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support. 		last database update
04/03/2013
MGI 5.12 		The Jackson Laboratory