Human Disease and Mouse Model Detail

Human Disease

Term: Myeloproliferative Disorder, Chronic, with Eosinophilia
OMIM ID: 131440

Synonyms

Eosinophils, Malignant Proliferation of; MPE; EMP

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...

Dok1	DOK1
Dok2	DOK2

...the mouse gene.
OMIM data currently do not associate this disease with the orthologous human gene.

PDGFRB

...the human gene.
MGI data currently do not associate this disease with mutations in the orthologous mouse gene.

Mouse Models

Genotype			Ref(s)
Allelic Composition	Note	Genetic Background
Models with phenotypic similarity to human disease where etiologies are distinct.¹
Dok1^tm1Ppp/Dok1^tm1Ppp Dok2^tm1Ppp/Dok2^tm1Ppp		129S1/Sv-Dok1^tm1Ppp Dok2^tm1Ppp	J:95334

¹Human genes are associated with this disease. Mouse model genotypes do not 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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