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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 | Abnormal cardiovascular system morphology |
Abnormal heart morphology |
Lumbosacral hemangioma |
| Disease(s) Associated with SMARCB1 | |||
| Coffin-Siris syndrome 3 | |||
| schwannomatosis |
| Mouse Phenotypes | bruising |
intestinal hemorrhage |
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| Availability | Mouse Genotype | ||
| Smarcb1tm1Sho/Smarcb1tm2Sho Tg(Mx1-cre)1Cgn/? (conditional) |
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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 05/21/2024 MGI 6.23 |
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