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Symbol
Name
ID

Smarcd1
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 1
MGI:1933623

Phenotype annotations related to digestive/alimentary system

Darker colors indicate more annotations

Human Phenotypes	Esophageal atresia
Disease(s) Associated with SMARCD1	Esophageal atresia
Coffin-Siris syndrome 11

Mouse Phenotypes		decreased intestinal cholesterol absorption	abnormal feces composition
Availability	Mouse Genotype
	Smarcd1^tm1.1Jddl/Smarcd1^tm1.1Jddl Speer6-ps1^{Tg(Alb-cre)21Mgn}/Speer6-ps1⁺ (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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