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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 nervous system

Darker colors indicate more annotations

Human Phenotypes	Dandy-Walker malformation	Microcephaly	Agenesis of corpus callosum	Absent speech	Intellectual disability	Global developmental delay	Seizure
Disease(s) Associated with SMARCA4
Coffin-Siris syndrome 4

Mouse Phenotypes		abnormal melanoblast morphology	exencephaly
Availability	Mouse Genotype	abnormal melanoblast morphology	exencephaly
	Smarca4^tm1Mag/Smarca4⁺
	Smarca4^tm1.2Pcn/Smarca4^tm1.2Pcn Tg(Sox10-cre)1Wdr/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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