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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Pxn
paxillin
MGI:108295
11 phenotypes from 1 allele in 1 genetic background
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Allelic Composition
Genetic Background
Annotated Term Reference
Pxntm1Smth/Pxntm1Smth
either: (involves: 129S4/SvJaeSor * C57BL/6) or (involves: 129/Sv)
abnormal allantois morphology J:73970
abnormal amnion morphology J:73970
abnormal dorsal aorta morphology J:73970
abnormal dorsal-ventral polarity of the somites J:73970
abnormal foregut morphology J:73970
abnormal heart development J:73970
absent cardiogenic plate J:73970
absent notochord J:73970
normal cellular phenotype J:73970
decreased embryo size J:73970
embryonic lethality during organogenesis, complete penetrance J:73970

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
04/23/2024
MGI 6.23
The Jackson Laboratory