About   Help   FAQ
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
Disease(s) Associated with MYCN
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
Mycntm1Fwa/Mycntm1Fwa
Mycntm1Knd/Mycntm1Knd
Mycntm1Par/Mycntm1Par
Mycntm1Jrt/Mycntm1Par
Mycntm1Nagy/Mycntm2.1Nagy
Mycntm1Psk/Mycntm1Psk
Tg(Nes-cre)1Kln/0  (conditional)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
04/09/2019
MGI 6.13
The Jackson Laboratory