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Human Disease and Mouse Model Detail
Human Disease

Term: Chediak-Higashi Syndrome; CHS
OMIM ID: 214500

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...
Lyst LYST
  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
Lystbg-14J/Lystbg-14J   C3Fe;B6-Lystbg-14J J:85200
Lystbg-2Btlr/Lystbg-2Btlr   C57BL/6J-Lystbg-2Btlr J:133617
Lystbg-Btlr/Lystbg-Btlr   C57BL/6J-Lystbg-Btlr J:133616
Lystbg-grey/Lystbg-grey   C57BL/6-Lystbg-grey J:106442
Lystbg-Lac/Lystbg-Lac   CBA/CaLac-Lystbg-Lac J:29745
Lystbg-slt/Lystbg-slt   YZ57/Ch J:25388
Lystbg/Lystbg   B6.C3Rl-Lystbg/J J:6801
Lystbg/Lystbg   B6.C3Rl-Lystbg 8

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
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last database update
04/03/2013
MGI 5.12
The Jackson Laboratory