Symbol Name ID |
Smarcb1
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 MGI:1328366 |
Darker colors indicate more annotations |
Human Phenotypes | Inguinal hernia |
Umbilical hernia |
Central diaphragmatic hernia |
Short stature |
Intrauterine growth retardation |
Disease(s) Associated with SMARCB1 | |||||
Coffin-Siris syndrome 3 |
Mouse Phenotypes | increased facial tumor incidence |
slow postnatal weight gain |
enlarged liver |
enlarged spleen |
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Availability | Mouse Genotype | ||||
Smarcb1em1Koke/Smarcb1em1Koke | |||||
Smarcb1tm1Gvk/Smarcb1+ | |||||
Smarcb1tm1Sho/Smarcb1tm3Sho Tg(Mx1-cre)1Cgn/? (conditional) |
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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