Symbol Name ID |
Smarcc2
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 2 MGI:1915344 |
Darker colors indicate more annotations |
Human Phenotypes | Inguinal hernia |
Failure to thrive |
Disease(s) Associated with SMARCC2 | ||
Coffin-Siris syndrome 8 |
Mouse Phenotypes | increased embryo weight |
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Availability | Mouse Genotype | |
Smarcc2tm1.2Stoy/Smarcc2tm1.2Stoy |
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 08/02/2024 MGI 6.24 |
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