86 phenotypes from 10 alleles in 13 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Erbb3m3329Ddg/Erbb3m3329Ddg involves: C3H/He * C57BL/6	abnormal axon fasciculation	J:159834
	abnormal dorsal root ganglion morphology	J:159834
	abnormal nervous system morphology	J:159834
Erbb3m3329Ddg/Erbb3m3329Ddg involves: C57BL/6	abnormal axon fasciculation	J:160880
	abnormal dorsal root ganglion morphology	J:160880
	abnormal mandibular nerve morphology	J:160880
	abnormal ophthalmic nerve morphology	J:160880
	abnormal spinal nerve morphology	J:160880
	embryonic lethality during organogenesis, incomplete penetrance	J:160880
	prenatal lethality, complete penetrance	J:160880
Erbb3m3329Ddg/Erbb3tm1Gne involves: 129S2/SvPas * C57BL/6	abnormal axon fasciculation	J:160880
	abnormal spinal nerve morphology	J:160880
	abnormal trigeminal nerve morphology	J:160880
Erbb3tm1.1(ERBB3)Mul/Erbb3tm1.1(ERBB3)Mul FVB.129P2(Cg)-Erbb3tm1.1(ERBB3)Mul	abnormal involution of the mammary gland	J:189292
	abnormal mammary gland alveolus morphology	J:189292
	abnormal mammary gland duct morphology	J:189292
	abnormal mammary gland epithelium morphology	J:189292
	abnormal mammary gland growth during lactation	J:189292
	decreased birth weight	J:189292
	decreased body weight	J:189292
	hypolactation	J:189292
	increased mammary gland apoptosis	J:189292
	postnatal growth retardation	J:189292
	preweaning lethality, incomplete penetrance	J:189292
Erbb3tm1.1Dwt/Erbb3tm1.1Dwt either: 129S6/SvEvTac-Erbb3tm1.1Dwt or B6.129S6-Erbb3tm1.1Dwt	lethality throughout fetal growth and development, incomplete penetrance	J:152703
	postnatal lethality, complete penetrance	J:152703
Erbb3tm1.1Dwt/Erbb3tm2.1Dwt involves: 129S6/SvEvTac * C57BL/6	no abnormal phenotype detected	J:152703
Erbb3tm1.1Dwt/Erbb3tm2.1Dwt Edil3Tg(Sox2-cre)1Amc/Edil3+ involves: 129S6/SvEvTac * C57BL/6 * CBA	preweaning lethality, complete penetrance	J:152703
Erbb3tm1.1Dwt/Erbb3tm2.1Dwt Tg(Vil1-cre)997Gum/0 involves: 129S6/SvEvTac * C57BL/6 * SJL	increased susceptibility to induced colitis	J:152703
Erbb3tm1.1Squ/Erbb3tm1.1Squ involves: 129S6/SvEvTac	no abnormal phenotype detected	J:114524
Erbb3tm1Cbm/Erbb3tm1Cbm either: 129P2/OlaHsd or (involves: 129P2/OlaHsd * C57BL/6)	abnormal cranial ganglia morphology	J:43515
	abnormal cranial nerve morphology	J:43515
	abnormal dorsal root ganglion morphology	J:43515
	abnormal PNS glial cell morphology	J:43515
	absent Schwann cell precursors	J:43515
	cyanosis	J:43515
	decreased body weight	J:43515
	embryonic lethality during organogenesis, incomplete penetrance	J:43515
	increased neuron apoptosis	J:43515
	motor neuron degeneration	J:43515
	neuron degeneration	J:43515
	no spontaneous movement	J:43515
	perinatal lethality, complete penetrance	J:43515
	respiratory failure	J:43515
	small dorsal root ganglion	J:43515
	unresponsive to tactile stimuli	J:43515
Erbb3tm1Gne/Erbb3tm1Gne involves: 129S2/SvPas * C57BL/6	abnormal atrioventricular valve development	J:45302
	abnormal brain morphology	J:45302
	abnormal brain ventricular system morphology	J:45302
	abnormal cardiac epithelial to mesenchymal transition	J:45302
	abnormal cerebellar plate morphology	J:45302
	abnormal cerebral aqueduct morphology	J:45302
	abnormal choroid plexus morphology	J:45302
	abnormal cranial flexure morphology	J:45302
	abnormal cranial ganglia morphology	J:45302
	abnormal embryonic neuroepithelial layer differentiation	J:45302
	abnormal enteric ganglia morphology	J:45302
	abnormal forebrain morphology	J:45302
	abnormal glial cell morphology	J:45302
	abnormal heart development	J:45302
	abnormal heart morphology	J:45302
	abnormal hindbrain morphology	J:45302
	abnormal midbrain morphology	J:45302
	abnormal myocardial trabeculae morphology	J:45302
	abnormal myocardium layer morphology	J:45302
	abnormal neocortex morphology	J:45302
	abnormal neuronal migration	J:45302
	abnormal pancreas morphology	J:45302
	abnormal pontine flexure morphology	J:45302
	abnormal stomach epithelium morphology	J:45302
	abnormal trigeminal ganglion morphology	J:45302
	abnormal ventral spinal root morphology	J:45302
	absent adrenergic chromaffin cells	J:45302
	absent cerebellum vermis	J:45302
	atrioventricular valve regurgitation	J:45302
	cerebellum hypoplasia	J:45302
	decreased Purkinje cell number	J:45302
	decreased Schwann cell number	J:45302
	embryonic lethality during organogenesis, complete penetrance	J:45302
	poor circulation	J:45302
	small nodose ganglion	J:45302
	small petrosal ganglion	J:45302
	thin atrioventricular cushion	J:45302
Erbb3tm1Squ/Erbb3tm1Squ Tg(EIIa-cre)C5379Lmgd/0 involves: 129S6/SvEvTac * FVB/N	abnormal atrioventricular valve morphology	J:114524
	abnormal dorsal root ganglion morphology	J:114524
	absent Schwann cells	J:114524
	embryonic lethality during organogenesis, incomplete penetrance	J:114524
Erbb3tm1Squ/Erbb3tm1Squ Tg(MMTV-cre)7Mul/0 involves: 129S6/SvEvTac * FVB/N	abnormal branching of the mammary ductal tree	J:114524
Erbb3tm2Cbm/Erbb3tm2Cbm either: 129P2/OlaHsd or (involves: 129P2/OlaHsd * C57BL/6)	abnormal cranial ganglia morphology	J:43515
	abnormal cranial nerve morphology	J:43515
	abnormal dorsal root ganglion morphology	J:43515
	abnormal PNS glial cell morphology	J:43515
	absent Schwann cell precursors	J:43515
	cyanosis	J:43515
	decreased body weight	J:43515
	embryonic lethality during organogenesis, incomplete penetrance	J:43515
	increased neuron apoptosis	J:43515
	motor neuron degeneration	J:43515
	neuron degeneration	J:43515
	no spontaneous movement	J:43515
	perinatal lethality, complete penetrance	J:43515
	respiratory failure	J:43515
	small dorsal root ganglion	J:43515
	unresponsive to tactile stimuli	J:43515
Erbb3tm2Cbm/Erbb3tm2Cbm involves: 129P2/OlaHsd	abnormal adrenal gland morphology	J:48515
	abnormal neural crest cell migration	J:48515
	abnormal paravertebral ganglion morphology	J:48515
	abnormal prevertebral ganglion morphology	J:48515
	abnormal superior cervical ganglion morphology	J:48515
	abnormal sympathetic ganglion morphology	J:48515
	abnormal sympathetic system morphology	J:48515
	absent adrenergic chromaffin cells	J:48515
	decreased noradrenaline level	J:48515
	small superior cervical ganglion	J:48515
Erbb3tm3Cbm/Erbb3tm3Cbm Tg(Dhh-cre)1Mejr/0 involves: 129P2/OlaHsd * FVB/N	absent Schwann cells	J:207470