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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Vim
vimentin
MGI:98932
25 phenotypes from multigenic genotypes
Export: Excel File
Allelic Composition
Genetic Background
Annotated Term Reference
Gfaptm1Pkny/Gfaptm1Pkny
Ppt1tm1Hof/Ppt1tm1Hof
Vimtm1Cba/Vimtm1Cba
involves: 129P2/OlaHsd * 129S2/SvPas * 129S6/SvEvTac * C57BL/6
abnormal brain morphology J:177265
abnormal cytokine level J:177265
abnormal nervous system morphology J:177265
abnormal visual cortex morphology J:177265
brain atrophy J:177265
brain inflammation J:177265
decreased brain weight J:177265
hippocampal neuron degeneration J:177265
neurodegeneration J:177265
premature death J:177265
thin cerebral cortex J:177265
Gfaptm1Pkny/Gfaptm1Pkny
Vimtm1Cba/Vimtm1Cba
involves: 129/Sv * 129P2/OlaHsd * C57BL/6
abnormal dentate gyrus morphology J:106195
abnormal neuron differentiation J:106195
Gfaptm1Pkny/Gfaptm1Pkny
Vimtm1Cba/Vimtm1Cba
involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6
abnormal astrocyte morphology J:125659
abnormal astrocyte physiology J:125659
abnormal spinal cord morphology J:124385
astrocytosis J:124385
decreased inflammatory response J:123278
decreased neuron apoptosis J:123278
gliosis J:123278
increased vasodilation J:124385
intracranial hemorrhage J:124385
normal nervous system phenotype J:124385
normal vision/eye phenotype J:123278
Gfaptm4Ito/Gfaptm4Ito
Vimtm1Cba/Vimtm1Cba
either: (involves: 129P2/OlaHsd * 129S2/SvPas) or (involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6)
abnormal astrocyte morphology J:78341
abnormal CNS glial cell morphology J:78341
Nestm1Dopa/Nestm1Dopa
Vimtm1Cba/Vimtm1Cba
involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6J
abnormal neuron differentiation J:168641

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
11/26/2019
MGI 6.14
The Jackson Laboratory