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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Smurf1
SMAD specific E3 ubiquitin protein ligase 1
MGI:1923038
7 phenotypes from 3 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
\Smurf1tm1b(EUCOMM)Wtsi/\Smurf1+
C57BL/6N-Smurf1tm1b(EUCOMM)Wtsi/H
trunk curl J:211773
\Smurf1tm1b(EUCOMM)Wtsi/\Smurf1tm1b(EUCOMM)Wtsi
C57BL/6N-Smurf1tm1b(EUCOMM)Wtsi/H
hyperactivity J:211773
\Smurf1tm1Wran/\Smurf1tm1Wran
involves: 129S1/Sv * 129X1/SvJ * ICR
no abnormal phenotype detected J:148693
\Smurf1tm1Yez/\Smurf1tm1Yez
either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * NIH Black Swiss)
abnormal osteoblast physiology J:97303
increased bone mineral density of femur J:97303
increased compact bone thickness J:97303
increased trabecular bone mass J:97303

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
03/25/2025
MGI 6.24
The Jackson Laboratory