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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Smarcc2
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 2
MGI:1915344
4 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
Pax6tm2Pgr/Pax6tm2Pgr
Smarcc2tm1.1Stoy/Smarcc2+
Emx1tm1(cre)Krj/Emx1+
involves: 129S1/Sv * 129S2/SvPas * C57BL/6
abnormal neuron number J:197141
normal nervous system phenotype J:197141
Pax6tm2Pgr/Pax6tm2Pgr
Smarcc2tm1.1Stoy/Smarcc2tm1.1Stoy
Emx1tm1(cre)Krj/Emx1+
involves: 129S1/Sv * 129S2/SvPas * C57BL/6
abnormal neocortex morphology J:197141
abnormal neuron number J:197141
abnormal neuronal precursor cell number J:197141

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