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Human Disease and Mouse Model Detail
Human Disease

Term: Stroke, Ischemic
OMIM ID: 601367

Synonyms Cerebral Infarction; Cerebrovascular Accident
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...
     
Alox5ap ALOX5AP
F2 F2
F5 F5
Nos3 NOS3
Prkch PRKCH
  human...the human gene.
     MGI data currently do not associate this disease with mutations in the orthologous mouse gene.
     

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
04/03/2013
MGI 5.12
The Jackson Laboratory