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Symbol
Name
ID
Mycn
v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived
MGI:97357
Phenotype annotations related to respiratory system
Darker colors indicate more annotations
Human Phenotypes
Tracheoesophageal fistula
Disease(s) Associated with MYCN
Feingold syndrome

Mouse Phenotypes
abnormal lung morphology
abnormal lung development
abnormal branching involved in lung morphogenesis
impaired branching involved in bronchus morphogenesis
abnormal lung epithelium morphology
abnormal pulmonary alveolus epithelial cell morphology
decreased type I pneumocyte number
decreased type II pneumocyte number
pulmonary hypoplasia
absent pulmonary alveoli
respiratory distress
respiratory failure
Availability Mouse Genotype
Mycntm1Jrt/Mycntm1Jrt
Mycntm1Knd/Mycntm1Knd
Mycntm1Par/Mycntm1Par
Mycntm1Jrt/Mycntm1Par
Mycntm1Nagy/Mycntm2.1Nagy
Tg(Sftpc-Nmyc1/EGFP)1Blh/0
Mycntm1Psk/Mycntm1Psk
Tg(Sftpc-cre)1Blh/0  (conditional)
Mycntm1Psk/Mycn+
Tg(Sftpc-cre)1Blh/0  (conditional)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
04/09/2019
MGI 6.13
The Jackson Laboratory