Pxn Phenotype Annotations

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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

Allelic Composition Genetic Background	Annotated Term	Reference
Pxn^tm1Smth/Pxn^tm1Smth 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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