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Symbol
Name
ID

Brd4
bromodomain containing 4
MGI:1888520

Phenotype annotations related to embryo

Darker colors indicate more annotations

Human Phenotypes	Increased nuchal translucency	Prenatal movement abnormality
Disease(s) Associated with BRD4	Increased nuchal translucency	Prenatal movement abnormality
Cornelia de Lange syndrome

Mouse Phenotypes		embryonic growth retardation	inner cell mass degeneration
Availability	Mouse Genotype	embryonic growth retardation	inner cell mass degeneration
	Brd4^{Gt(pGT1.8TM)ST132Nimr}/Brd4^{Gt(pGT1.8TM)ST132Nimr}
	Brd4^{Gt(pGT1.8TM)ST132Nimr}/Brd4⁺

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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