Symbol
Name
ID

Mycn
v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived
MGI:97357

Phenotype annotations related to cardiovascular system

Darker colors indicate more annotations

Human Phenotypes	Ventricular septal defect	Tricuspid atresia	Interrupted aortic arch	Patent ductus arteriosus	Tricuspid stenosis	Abnormality of the spleen	Asplenia	Accessory spleen	Polysplenia
Disease(s) Associated with MYCN
Feingold syndrome

Mouse Phenotypes

abnormal dorsal aorta morphology

dilated dorsal aorta

abnormal angiogenesis

abnormal anterior cardinal vein morphology

absent vitelline blood vessels

abnormal vein morphology

trabecula carnea hypoplasia

thin myocardium compact layer

thin myocardium

abnormal cardiac epithelial to mesenchymal transition

abnormal heart development

common ventricle

small heart

hemorrhage

abnormal fetal cardiomyocyte proliferation

congestive heart failure

Availability

Mouse Genotype

Mycn^tm1Fwa/Mycn^tm1Fwa

Mycn^tm1Knd/Mycn^tm1Knd

Mycn^tm1Par/Mycn^tm1Par

Mycn^tm1Jrt/Mycn^tm1Par

Mycn^tm1Nagy/Mycn^tm2.1Nagy

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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