106 phenotypes from 11 alleles in 9 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Mycntm1.1Nagy/Mycntm1.1Nagy involves: 129S1/Sv * 129X1/SvJ	no abnormal phenotype detected	J:67930
Mycntm1.1Psk/Mycntm1.1Psk involves: 129 * C57BL/6	prenatal lethality, complete penetrance	J:79489
Mycntm1Fwa/Mycntm1Fwa involves: 129S/SvEv	abnormal liver development	J:46520
	abnormal liver morphology	J:46520
	decreased hematopoietic stem cell number	J:46520
	increased hepatocyte apoptosis	J:46520
	liver hypoplasia	J:46520
	small liver	J:46520
Mycntm1Fwa/Mycntm1Fwa involves: 129S/SvEv * MF1	abnormal anterior cardinal vein morphology	J:3413
	abnormal cardiac epithelial to mesenchymal transition	J:3413
	abnormal cranial ganglia morphology	J:3413
	abnormal embryonic neuroepithelium morphology	J:3413
	abnormal heart development	J:3413
	abnormal lens vesicle development	J:3413
	abnormal mesonephros morphology	J:3413
	abnormal optic vesicle formation	J:3413
	decreased embryo size	J:3413
	dorsal root ganglion hypoplasia	J:3413
	embryonic lethality during organogenesis, complete penetrance	J:3413
	small dorsal root ganglion	J:3413
	small trigeminal ganglion	J:3413
	trabecula carnea hypoplasia	J:3413
Mycntm1Jrt/Mycntm1Jrt involves: 129S2/SvPas * C57BL/6J	abnormal lung morphology	J:973
	neonatal lethality, complete penetrance	J:973
	no spontaneous movement	J:973
	respiratory distress	J:973
Mycntm1Jrt/Mycntm1Par involves: 129S2/SvPas * C57BL/6J	abnormal fetal cardiomyocyte proliferation	J:15281
	abnormal vein morphology	J:15281
	congestive heart failure	J:15281
	decreased embryo size	J:15281
	decreased fetal size	J:15281
	edema	J:15281
	embryonic lethality during organogenesis, complete penetrance	J:15281
	impaired branching involved in bronchus morphogenesis	J:15281
	normal nervous system phenotype	J:15281
	normal reproductive system phenotype	J:15281
	small heart	J:15281
	small kidney	J:15281
	thin myocardium	J:15281
	thin myocardium compact layer	J:15281
Mycntm1Knd/Mycntm1Knd involves: 129P2/OlaHsd * BALB/c	abnormal apical ectodermal ridge morphology	J:11859
	abnormal brain morphology	J:11859
	abnormal limb bud morphology	J:11859
	abnormal limb development	J:11859
	abnormal liver development	J:11859
	abnormal neural tube morphology	J:11859
	abnormal stomach morphology	J:11859
	common ventricle	J:11859
	decreased body length	J:11859
	embryonic lethality during organogenesis, complete penetrance	J:11859, J:76279
	impaired branching involved in bronchus morphogenesis	J:11859
	normal nervous system phenotype	J:11859
	small dorsal root ganglion	J:11859
	small heart	J:11859
	small liver	J:11859
	thin myocardium	J:11859
	trabecula carnea hypoplasia	J:11859
Mycntm1Nagy/Mycntm1Nagy involves: 129S1/Sv * 129X1/SvJ	vertebral fusion	J:67930
Mycntm1Nagy/Mycntm2.1Nagy involves: 129S1/Sv * 129X1/SvJ	abnormal angiogenesis	J:67930
	abnormal lung development	J:67930
	abnormal vertebrae morphology	J:67930
	abnormal vertebral body development	J:67930
	absent vitelline blood vessels	J:67930
	decreased embryo size	J:67930
	neonatal lethality, complete penetrance	J:67930
	pale yolk sac	J:67930
	respiratory failure	J:67930
	small vertebral body	J:67930
	thin myocardium	J:67930
	vertebral fusion	J:67930
Mycntm1Par/Mycn+ involves: 129S2/SvPas * C57BL/6J	postnatal lethality, incomplete penetrance	J:3432
Mycntm1Par/Mycntm1Par involves: 129S2/SvPas * C57BL/6J	abnormal cranial ganglia morphology	J:3432
	abnormal dorsal aorta morphology	J:3432
	abnormal embryo development	J:3432
	abnormal embryonic neuroepithelial layer differentiation	J:3432
	abnormal forebrain development	J:3432
	abnormal intestinal epithelium morphology	J:3432
	abnormal large intestine morphology	J:3432
	abnormal lung development	J:3432
	abnormal medulla oblongata morphology	J:3432
	abnormal mesonephric mesenchyme morphology	J:3432
	abnormal mesonephros morphology	J:3432
	abnormal Wolffian duct morphology	J:3432
	absent stomach	J:3432
	anemia	J:3432
	decreased embryo size	J:3432
	dilated dorsal aorta	J:3432
	disorganized dorsal root ganglion	J:3432
	embryonic growth arrest	J:3432
	embryonic growth retardation	J:3432
	embryonic lethality during organogenesis, complete penetrance	J:3432
	first pharyngeal arch hypoplasia	J:3432
	gonadal ridge hypoplasia	J:3432
	hemorrhage	J:3432
	impaired branching involved in bronchus morphogenesis	J:3432
	pulmonary hypoplasia	J:3432
	small dorsal root ganglion	J:3432
	small trigeminal ganglion	J:3432
	telencephalon hypoplasia	J:3432
	thin myocardium	J:3432
Mycntm1Psk/Mycn+ Tg(Sftpc-cre)1Blh/0 involves: 129 * C57BL/6 * ICR	abnormal branching involved in lung morphogenesis	J:97215
	abnormal lung development	J:97215
	abnormal lung epithelium morphology	J:97215
	abnormal lung morphology	J:97215
	decreased survivor rate	J:97215
	decreased type I pneumocyte number	J:97215
	decreased type II pneumocyte number	J:97215
	neonatal lethality, incomplete penetrance	J:97215
Mycntm1Psk/Mycntm1Psk Tg(Nes-cre)1Kln/0 involves: 129 * C57BL/6 * SJL	abnormal cerebellar foliation	J:79489
	abnormal cerebellar granule layer morphology	J:79489
	abnormal cerebellar molecular layer	J:79489
	abnormal cerebellar Purkinje cell layer	J:79489
	abnormal cerebellum development	J:79489
	abnormal cerebellum external granule cell layer morphology	J:79489
	abnormal cerebellum morphology	J:79489
	abnormal cerebral cortex morphology	J:79489
	abnormal cortical ventricular zone morphology	J:79489
	abnormal embryonic neuroepithelium morphology	J:79489
	abnormal neuron differentiation	J:79489
	abnormal neuronal precursor proliferation	J:79489
	decreased brain size	J:79489
	decreased embryonic neuroepithelium thickness	J:79489
	decreased neuronal precursor cell number	J:79489
	decreased Purkinje cell number	J:79489
	ectopic Purkinje cell	J:79489
	microcephaly	J:79489
	microphthalmia	J:79489
	normal nervous system phenotype	J:79489
	postnatal growth retardation	J:79489
	premature neuronal precursor differentiation	J:79489
	small cerebellum	J:79489
Mycntm1Psk/Mycntm1Psk Tg(Sftpc-cre)1Blh/0 involves: 129 * C57BL/6 * ICR	abnormal branching involved in lung morphogenesis	J:97215
	abnormal lung development	J:97215
	abnormal lung epithelium morphology	J:97215
	abnormal lung morphology	J:97215
	abnormal pulmonary alveolus epithelial cell morphology	J:97215
	decreased type I pneumocyte number	J:97215
	decreased type II pneumocyte number	J:97215
	neonatal lethality, complete penetrance	J:97215
Mycntm2.1Nagy/Mycn+ involves: 129S1/Sv * 129X1/SvJ	kinked tail	J:67930
	vertebral fusion	J:67930
Mycntm2.1Nagy/Mycntm2.1Nagy involves: 129S1/Sv * 129X1/SvJ	embryonic lethality during organogenesis, complete penetrance	J:67930
Mycntm2Nagy/Mycn+ involves: 129S1/Sv * 129X1/SvJ	kinked tail	J:67930
Mycntm2Nagy/Mycntm2Nagy involves: 129S1/Sv * 129X1/SvJ	embryonic lethality during organogenesis, complete penetrance	J:67930
Tg(Sftpc-Nmyc1/EGFP)1Blh/0 involves: C57BL/6 * DBA	abnormal lung development	J:97215
	absent pulmonary alveoli	J:97215