Usp39 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Usp39
ubiquitin specific peptidase 39
MGI:107622

8 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Usp39^em1Imat/Usp39^em1Imat CD1-Usp39^em1Imat	abnormal developmental patterning	J:324183
	abnormal embryo morphology	J:324183
	abnormal embryonic epiblast morphology	J:324183
	abnormal mesoderm development	J:324183
	embryonic lethality, complete penetrance	J:324183
	failure of primitive streak formation	J:324183
Usp39^{tm1b(EUCOMM)Hmgu}/Usp39⁺ C57BL/6N-Usp39^{tm1b(EUCOMM)Hmgu}/Nju	abnormal auditory brainstem response	J:211773
	abnormal coat/hair pigmentation	J:211773

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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