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 | Facial palsy |
Macroglossia |
Foot dorsiflexor weakness |
Wrist drop |
Central diaphragmatic hernia |
Hypotonia |
Muscle weakness |
Disease(s) Associated with SMARCB1 | |||||||
atypical teratoid rhabdoid tumor | |||||||
Coffin-Siris syndrome 3 | |||||||
schwannomatosis | |||||||
vestibular schwannomatosis |
Mouse Phenotypes | increased rhabdomyoma incidence |
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Availability | Mouse Genotype | |
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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