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Symbol
Name
ID

Smarca4
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4
MGI:88192

Phenotype annotations related to muscle

Darker colors indicate more annotations

Human Phenotypes	Macroglossia	Hypotonia
Disease(s) Associated with SMARCA4	Macroglossia	Hypotonia
Coffin-Siris syndrome 4

Mouse Phenotypes		thick myocardium	cardiomyopathy	abnormal intestinal smooth muscle morphology	abnormal muscle physiology	impaired smooth muscle contractility
Availability	Mouse Genotype	thick myocardium	cardiomyopathy	abnormal intestinal smooth muscle morphology	abnormal muscle physiology	impaired smooth muscle contractility
	Nfatc1^tm1.1(cre)Bz/Nfatc1⁺ Smarca4^tm1.2Pcn/Smarca4^tm1.2Pcn (conditional)
	Nfatc1^tm1(cre)Bz/Nfatc1⁺ Smarca4^tm1.2Pcn/Smarca4^tm1.2Pcn (conditional)
	Smarca4^tm1.2Pcn/Smarca4^tm1.1Pcn Tg(Myh11-cre,-EGFP)2Mik/0 (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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