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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 growth/size/body

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
Availability	Mouse Genotype	increased facial tumor incidence	slow postnatal weight gain	enlarged liver	enlarged spleen
	Smarcb1^em1Koke/Smarcb1^em1Koke
	Smarcb1^tm1Gvk/Smarcb1⁺
	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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