46 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Emx2tm1Sia/Emx2tm1Sia Pax6Sey/Pax6Sey involves: C57BL/6 * CBA	abnormal Ammon gyrus morphology	J:98539
	abnormal brain commissure morphology	J:98539
	abnormal brain morphology	J:98539
	abnormal cerebral cortex morphology	J:98539
	abnormal embryonic/fetal subventricular zone morphology	J:98539
	abnormal pretectal region morphology	J:98539
	abnormal tectum morphology	J:98539
	abnormal telencephalon morphology	J:98539
	abnormal thalamus morphology	J:98539
	absent choroid plexus	J:98539
	absent diencephalon	J:98539
	absent hippocampus	J:98539
Gli2tm1Alj/Gli2tm1Alj Pax6Sey/Pax6Sey involves: 129S1/Sv * 129X1/SvJ	abnormal neuron differentiation	J:112802
Mitfmi-vga9/Mitf+ Pax6Sey-Neu/Pax6+ involves: C57BL/6 * CBA	abnormal retina pigment epithelium morphology	J:188155
Mitfmi-vga9/Mitfmi-vga9 Pax6Sey-Neu/Pax6+ involves: C57BL/6 * CBA	abnormal retina pigment epithelium morphology	J:188155
Mitfmi-vga9/Mitfmi-vga9 Pax6Sey-Neu/Pax6Sey-Neu involves: C57BL/6 * CBA	abnormal retina pigment epithelium morphology	J:188155
Mitftm3.1Arnh/Mitftm3.1Arnh Pax6Sey-Neu/Pax6+ involves: 129S6/SvEvTac * C57BL/6N	abnormal retina pigment epithelium morphology	J:188155
Pax6Sey-H/Pax6+ involves: 101/H * C3H/HeH	belly spot	J:8534
	coloboma	J:8534
	decreased body size	J:8534
	lowered ear position	J:8534
	microphthalmia	J:8534
	reduced female fertility	J:8534
	small ears	J:8534
Pax6Sey-H/Pax6Sey-H involves: 101/H * C3H/HeH	embryonic lethality, complete penetrance	J:8534
Pax6Sey-Neu/Pax6+ Sox2tm1.1Vep/Sox2+ involves: 102 * C3H * C3H/HeN	abnormal lens morphology	J:119175
Pax6Sey/Pax6Sey-H involves: 101/H * C3H/HeH * C57BL/10	abnormal face development	J:8534
	abnormal maxillary shelf morphology	J:8534
	absent snout	J:8534
	anophthalmia	J:8534
	decreased embryo size	J:8534
Pax6Sey/Pax6Sey-Neu Tg(Hbb-b1)83Clo/0 involves: 102 * C3H * C57BL * CBA/Ca * CD-1 * SJL	abnormal craniofacial bone morphology	J:43913
	abnormal nasal capsule morphology	J:43913
	supernumerary incisors	J:43913
Pax6Sey/Pax6Sey Tg(Hbb-b1)83Clo/0 involves: C57BL * CBA/Ca * CD-1 * SJL	abnormal craniofacial bone morphology	J:43913
	abnormal nasal capsule morphology	J:43913
	supernumerary incisors	J:43913
Pax6Sey/Pax6Sey Tg(PAX6)77Ndha/? involves: C57BL/6 * CBA	normal nervous system phenotype	J:34194
	normal taste/olfaction phenotype	J:34194
	normal vision/eye phenotype	J:34194
Pax6tm2(Pax6_i5a,Pax2)Xzh/Pax6+ involves: 129S6/SvEvTac	normal vision/eye phenotype	J:198381
Pax6tm2(Pax6_i5a,Pax2)Xzh/Pax6tm2(Pax6_i5a,Pax2)Xzh involves: 129S6/SvEvTac	abnormal eye development	J:198381
	abnormal neuronal precursor proliferation	J:198381
	abnormal retina development	J:198381
	abnormal telencephalon development	J:198381
	thin cortical plate	J:198381
Pax6tm2.1(Pax6_i5a,Pax2)Xzh/Pax6+ involves: 129S6/SvEvTac * C57BL/6 * FVB/N	corneal-lenticular stalk	J:198381
Pax6tm2.1(Pax6_i5a,Pax2)Xzh/Pax6tm2.1(Pax6_i5a,Pax2)Xzh involves: 129S6/SvEvTac * C57BL/6 * FVB/N	abnormal cortical plate morphology	J:198381
	abnormal eye development	J:198381
	abnormal neuronal precursor proliferation	J:198381
	abnormal retina development	J:198381
	abnormal telencephalon development	J:198381
Pax6tm2Pgr/Pax6tm2Pgr Smarcc2tm1.1Stoy/Smarcc2+ Emx1tm1(cre)Krj/Emx1+ involves: 129S1/Sv * 129S2/SvPas * C57BL/6	abnormal neuron number	J:197141
	normal nervous system phenotype	J:197141
Pax6tm2Pgr/Pax6tm2Pgr Smarcc2tm1.1Stoy/Smarcc2tm1.1Stoy Emx1tm1(cre)Krj/Emx1+ involves: 129S1/Sv * 129S2/SvPas * C57BL/6	abnormal neocortex morphology	J:197141
	abnormal neuron number	J:197141
	abnormal neuronal precursor cell number	J:197141
Pax6tm2Pgr/Pax6tm2Pgr Sox2tm1.1Lan/Sox2tm1.1Lan Tg(Cryaa-cre)10Mlr/0 involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N * SJL	abnormal lens epithelium morphology	J:152850
	increased lens epithelium apoptosis	J:152850
	microphthalmia	J:152850