Human Disease and Mouse Model Detail

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Human Disease

Term: Pick Disease of Brain
OMIM ID: 172700

Synonyms

Dementia with Lobar Atrophy and Neuronal Cytoplasmic Inclusions; Lobar Atrophy of Brain

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...

Mapt	MAPT
Psen1	PSEN1

...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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