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Symbol
Name
ID

Ehmt1
euchromatic histone methyltransferase 1
MGI:1924933

Phenotype annotations related to cardiovascular system

Darker colors indicate more annotations

Human Phenotypes	Ventricular septal defect	Conotruncal defect	Tetralogy of Fallot	Bicuspid aortic valve	Coarctation of aorta	Pulmonary artery stenosis	Arrhythmia
Disease(s) Associated with EHMT1
Kleefstra syndrome 1

Mouse Phenotypes		abnormal retina vasculature morphology	abnormal retina blood vessel morphology	decreased atrioventricular cushion size	abnormal mitral valve cusp morphology	absent tricuspid valve cusps	atrioventricular septal defect
Availability	Mouse Genotype	abnormal retina vasculature morphology	abnormal retina blood vessel morphology	decreased atrioventricular cushion size	abnormal mitral valve cusp morphology	absent tricuspid valve cusps	atrioventricular septal defect
	Ehmt1^{tm1b(EUCOMM)Hmgu}/Ehmt1⁺
	Ehmt1^tm2Yshk/Ehmt1^tm2Yshk Nkx2-5^tm1(cre)Rjs/Nkx2-5⁺ (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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