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Symbol
Name
ID
Mycn
v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived
MGI:97357
Phenotype annotations related to behavior/neurological
Darker colors indicate more annotations
Human Phenotypes
Decreased fetal movement
Vocal cord paralysis
Disease(s) Associated with MYCN
Feingold syndrome

Mouse Phenotypes
no spontaneous movement
Availability Mouse Genotype
Mycntm1Jrt/Mycntm1Jrt

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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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory