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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Usp8
ubiquitin specific peptidase 8
MGI:1934029
12 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Usp8tm1.1Kpk/Usp8tm1.1Kpk
Tg(Mx1-cre)1Cgn/0
involves: 129P2/OlaHsd * C57BL/6 * CBA * FVB/N
abnormal hepatocyte morphology J:122732
hepatic necrosis J:122732
increased circulating bilirubin level J:122732
increased hepatocyte apoptosis J:122732
jaundice J:122732
liver failure J:122732
premature death J:122732
Usp8tm1.2Kpk/Usp8tm1.2Kpk
involves: 129P2/OlaHsd * FVB/N
abnormal dorsal-ventral axis patterning J:122732
abnormal embryo development J:122732
abnormal heart development J:122732
embryonic growth retardation J:122732
embryonic lethality, complete penetrance J:122732

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