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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
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Allelic Composition
Genetic Background
Annotated Term Reference
Usp39em1Imat/Usp39em1Imat
CD1-Usp39em1Imat
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
Usp39tm1b(EUCOMM)Hmgu/Usp39+
C57BL/6N-Usp39tm1b(EUCOMM)Hmgu/Nju
abnormal auditory brainstem response J:211773
abnormal coat/hair pigmentation J:211773

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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