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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Tor1b
torsin family 1, member B
MGI:1353605
6 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
Tor1atm1Wtd/Tor1atm3.1Wtd
Tor1btm1.2Wtd/Tor1btm1.1Wtd
Emx1tm1(cre)Krj/Emx1+
involves: 129S1/Sv * 129S2/SvPas * 129S6/SvEvTac * C57BL/6J
gliosis J:288753
neurodegeneration J:288753
postnatal growth retardation J:288753
premature death J:288753
thin cerebral cortex J:288753
Tor1atm2Wtd/Tor1atm3.1Wtd
Tor1btm1.2Wtd/Tor1b+
Emx1tm1(cre)Krj/Emx1+
involves: 129S1/Sv * 129S2/SvPas * 129S6/SvEvTac * C57BL/6J
limb grasping J:288753
thin cerebral cortex J:288753
Tor1atm2Wtd/Tor1atm3.1Wtd
Tor1btm1.2Wtd/Tor1btm1.2Wtd
Emx1tm1(cre)Krj/Emx1+
involves: 129S1/Sv * 129S2/SvPas * 129S6/SvEvTac * C57BL/6J
thin cerebral cortex J:288753

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
04/16/2024
MGI 6.23
The Jackson Laboratory