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Human Disease and Mouse Model Detail
Human Disease

Term: Inclusion Body Myositis
OMIM ID: 147421

Synonyms IBM
Transgenes and
other mutation types
Tg(Ckm-APPSw)A2Lfa   Characteristics of this human disease are associated with transgenes and other mutation types in mouse.
Tg(Ckm-APPSw)A6Lfa

Mouse Models
Genotype Ref(s)
Allelic Composition Note Genetic Background
Models involving transgenes or other mutation types.1
Tg(Ckm-APPSw)A2Lfa/0   involves: C57BL/6 * SJL J:76338
Tg(Ckm-APPSw)A6Lfa/0   involves: C57BL/6 * SJL J:76338

1Models involving transgenes or other mutation types may also appear in other sections of the table.
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
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Send questions and comments to User Support. 		last database update
04/03/2013
MGI 5.12 		The Jackson Laboratory