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Symbol
Name
ID

Brd4
bromodomain containing 4
MGI:1888520

Phenotype annotations related to vision/eye

Darker colors indicate more annotations

Human Phenotypes	Blepharitis	Microcornea	Cataract	Phthisis bulbi	Strabismus	Nystagmus	Myopia	Glaucoma	Ptosis
Disease(s) Associated with BRD4
Cornelia de Lange syndrome

Mouse Phenotypes		abnormal retina blood vessel morphology	abnormal eye posterior chamber depth	cataract	microphthalmia	abnormal retina inner nuclear layer morphology	abnormal retina outer nuclear layer morphology	decreased total retina thickness
Availability	Mouse Genotype	abnormal retina blood vessel morphology	abnormal eye posterior chamber depth	cataract	microphthalmia	abnormal retina inner nuclear layer morphology	abnormal retina outer nuclear layer morphology	decreased total retina thickness
	Brd4^{Gt(pGT1.8TM)ST132Nimr}/Brd4⁺
	Brd4^{tm1b(EUCOMM)Wtsi}/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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