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Symbol
Name
ID
Mycn
v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived
MGI:97357
Phenotype annotations related to craniofacial
Darker colors indicate more annotations
Human Phenotypes
Prominent occiput
Micrognathia
Microcephaly
Secondary microcephaly
Small anterior fontanelle
Facial asymmetry
Triangular face
Everted lower lip vermilion
Thick vermilion border
High palate
Orofacial cleft
Anteverted nares
Depressed nasal tip
Depressed nasal bridge
Wide nasal bridge
Blepharophimosis
Narrow palpebral fissure
Short palpebral fissure
Upslanted palpebral fissure
Epicanthus
Disease(s) Associated with MYCN
Feingold syndrome

Mouse Phenotypes
first pharyngeal arch hypoplasia
Availability Mouse Genotype
Mycntm1Par/Mycntm1Par

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