Symbol
Name
ID

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

Phenotype annotations related to embryo

Darker colors indicate more annotations

Human Phenotypes	Polyhydramnios	Decreased fetal movement
Disease(s) Associated with MYCN	Polyhydramnios	Decreased fetal movement
Feingold syndrome

Mouse Phenotypes

absent vitelline blood vessels

first pharyngeal arch hypoplasia

abnormal embryo development

embryonic growth arrest

embryonic growth retardation

decreased embryo size

abnormal apical ectodermal ridge morphology

gonadal ridge hypoplasia

abnormal limb bud morphology

abnormal mesonephros morphology

abnormal Wolffian duct morphology

abnormal neural tube morphology

abnormal embryonic neuroepithelium morphology

abnormal embryonic neuroepithelial layer differentiation

decreased embryonic neuroepithelium thickness

pale yolk sac

Availability

Mouse Genotype

Mycn^tm1Fwa/Mycn^tm1Fwa

Mycn^tm1Knd/Mycn^tm1Knd

Mycn^tm1Par/Mycn^tm1Par

Mycn^tm1Jrt/Mycn^tm1Par

Mycn^tm1Nagy/Mycn^tm2.1Nagy

Mycn^tm1Psk/Mycn^tm1Psk
Tg(Nes-cre)1Kln/0 (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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