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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Barx2
BarH-like homeobox 2
MGI:109617
14 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
Barx2tm1Rsd/Barx2tm1Rsd
Dmdmdx/Y
involves: 129 * C57BL/6 * C57BL/10ScSn
abnormal diaphragm morphology J:187799
abnormal gait J:187799
decreased body size J:187799
decreased locomotor activity J:187799
decreased muscle weight J:187799
impaired skeletal muscle regeneration J:187799
increased variability of skeletal muscle fiber size J:187799
kyphosis J:187799
postnatal lethality, incomplete penetrance J:187799
progressive muscle weakness J:187799
skeletal muscle endomysial fibrosis J:187799
skeletal muscle fiber necrosis J:187799
skeletal muscle fibrosis J:187799
thin diaphragm muscle J:187799
Barx2tm1Rsd/Barx2tm1Rsd
Dmdmdx/Dmdmdx
involves: 129 * C57BL/6 * C57BL/10ScSn
abnormal diaphragm morphology J:187799
abnormal gait J:187799
decreased body size J:187799
decreased locomotor activity J:187799
decreased muscle weight J:187799
impaired skeletal muscle regeneration J:187799
increased variability of skeletal muscle fiber size J:187799
kyphosis J:187799
postnatal lethality, incomplete penetrance J:187799
progressive muscle weakness J:187799
skeletal muscle endomysial fibrosis J:187799
skeletal muscle fiber necrosis J:187799
skeletal muscle fibrosis J:187799
thin diaphragm muscle J:187799

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory