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Symbol
Name
ID

Smarcc2
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 2
MGI:1915344

Phenotype annotations related to nervous system

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Thin corpus callosum	Cerebral atrophy	Absent speech	Delayed speech and language development	Aggressive behavior	Hyperactivity	Self-injurious behavior	Intellectual disability	Sleep abnormality	Global developmental delay	Seizure
Disease(s) Associated with SMARCC2
Coffin-Siris syndrome 8

Mouse Phenotypes		nervous system phenotype	abnormal neuron differentiation	abnormal neuronal precursor proliferation	abnormal neocortex morphology	thickened cerebral cortex	thin cerebral cortex	abnormal neuron number	abnormal neuronal precursor cell number
Availability	Mouse Genotype	nervous system phenotype	abnormal neuron differentiation	abnormal neuronal precursor proliferation	abnormal neocortex morphology	thickened cerebral cortex	thin cerebral cortex	abnormal neuron number	abnormal neuronal precursor cell number
	Smarcc2^tm1.1Stoy/Smarcc2^tm1.1Stoy (conditional)
	Smarcc2^tm1.1Stoy/Smarcc2^tm1.1Stoy Emx1^tm1(cre)Krj/Emx1⁺ (conditional)
	Smarcc2^tm1.1Stoy/Smarcc2^tm1.1Stoy Neurod6^tm1(cre)Kan/Neurod6⁺ (conditional)	*
	Emx1^tm1(cre)Krj/Emx1⁺ Tg(CMV-GFP,-Smarcc2,-lacZ)#Stoy/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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