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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
Macroglossia
Generalized hypotonia
Disease(s) Associated with SMARCB1
Coffin-Siris syndrome 3

Mouse Phenotypes
increased rhabdomyoma incidence
Availability Mouse Genotype
Smarcb1tm1Sho/Smarcb1tm3Sho
Tg(Mx1-cre)1Cgn/?  (conditional)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
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last database update
12/04/2018
MGI 6.13
The Jackson Laboratory