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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Gjc2
gap junction protein, gamma 2
MGI:2153060
15 phenotypes from 3 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Gjc2tm1(EGFP)Kwi/Gjc2tm1(EGFP)Kwi
involves: 129P2/OlaHsd * C57BL/6
abnormal brain morphology J:83885
abnormal cerebellum morphology J:174197
abnormal cerebellum white matter morphology J:174197
abnormal myelination J:83885, J:174197
abnormal oligodendrocyte physiology J:174197
astrocytosis J:174197
microgliosis J:174197
neurodegeneration J:83885
Gjc2tm1Paul/Gjc2tm1Paul
involves: 129/Sv * C57BL/6
no abnormal phenotype detected J:84338
Gjc2tm2.1Kwi/Gjc2+
involves: C57BL/6 * SJL
abnormal brain white matter morphology J:174197
abnormal cerebellum morphology J:174197
abnormal oligodendrocyte physiology J:174197
decreased locomotor activity J:174197
decreased vertical activity J:174197
increased oligodendrocyte number J:174197
microgliosis J:174197
Gjc2tm2.1Kwi/Gjc2tm2.1Kwi
involves: C57BL/6 * SJL
abnormal brain white matter morphology J:174197
abnormal cerebellum morphology J:174197
abnormal cerebellum white matter morphology J:174197
abnormal motor learning J:174197
abnormal myelination J:174197
abnormal oligodendrocyte physiology J:174197
astrocytosis J:174197
increased oligodendrocyte number J:174197
microgliosis J:174197
Purkinje cell degeneration J:174197

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
04/09/2024
MGI 6.23
The Jackson Laboratory