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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 04/23/2024 MGI 6.23 |
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