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Symbol
Name
ID

Smarcb1
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1
MGI:1328366

Phenotype annotations related to muscle

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	Facial palsy	Macroglossia	Foot dorsiflexor weakness	Wrist drop	Central diaphragmatic hernia	Hypotonia	Muscle weakness
atypical teratoid rhabdoid tumor
Coffin-Siris syndrome 3
schwannomatosis
vestibular schwannomatosis

Mouse Phenotypes		increased rhabdomyoma incidence
Availability	Mouse Genotype	increased rhabdomyoma incidence
	Smarcb1^tm1Sho/Smarcb1^tm3Sho Tg(Mx1-cre)1Cgn/? (conditional)

Contributing Projects: 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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