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Symbol
Name
ID

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

Phenotype annotations related to digestive/alimentary system

Darker colors indicate more annotations

Human Phenotypes	Esophageal atresia	Tracheoesophageal fistula	Duodenal atresia	Jejunal atresia	Intestinal atresia	Gastrointestinal atresia
Disease(s) Associated with MYCN
Feingold syndrome

Mouse Phenotypes		abnormal intestinal epithelium morphology	abnormal large intestine morphology	abnormal stomach morphology	absent stomach
Availability	Mouse Genotype	abnormal intestinal epithelium morphology	abnormal large intestine morphology	abnormal stomach morphology	absent stomach
	Mycn^tm1Knd/Mycn^tm1Knd
	Mycn^tm1Par/Mycn^tm1Par

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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