23 phenotypes from 6 alleles in 8 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
FusGt(U3NeoSV1)HO14Ggh/FusGt(U3NeoSV1)HO14Ggh B6.129S2-FusGt(U3NeoSV1)HO14Ggh	abnormal chromosome morphology	J:60213
	abnormal immunoglobulin level	J:60213
	abnormal suckling behavior	J:60213
	aneuploidy	J:60213
	chromosome breakage	J:60213
	decreased B cell number	J:60213
	decreased lymphocyte cell number	J:60213
	lymphoid hypoplasia	J:60213
	neonatal lethality, complete penetrance	J:60213
	small thymus	J:60213
FusGt(U3NeoSV1)HO14Ggh/FusGt(U3NeoSV1)HO14Ggh involves: 129S2/SvPas	abnormal hippocampus pyramidal cell morphology	J:97092
Fustm1.1(KOMP)Vlcg/Fus+ C57BL/6N-Fustm1.1(KOMP)Vlcg/Ucd	increased prepulse inhibition	J:211773
	increased respiratory quotient	J:211773
Fustm1.1(KOMP)Vlcg/Fustm1.1(KOMP)Vlcg C57BL/6N-Fustm1.1(KOMP)Vlcg/Ucd	abnormal embryo size	J:211773
	preweaning lethality, complete penetrance	J:211773
Fustm1.1Emcf/Fus+ involves: C3H * C57BL/6J * C57BL/6N	abnormal gait	J:249965
	abnormal neuromuscular synapse morphology	J:249965
	decreased motor neuron number	J:249965
	impaired limb coordination	J:249965
	motor neuron degeneration	J:249965
	premature death	J:249965
Fustm1a(EUCOMM)Wtsi/Fustm1c(EUCOMM)Wtsi Chattm2(cre)Lowl/Chat+ involves: 129S6/SvEvTac * C3H * C57BL/6 * C57BL/6N	normal nervous system phenotype	J:232167
Fustm1a(EUCOMM)Wtsi/Fustm1c(EUCOMM)Wtsi Ndor1Tg(UBC-cre/ERT2)1Ejb/0 involves: 129S/SvEv * C3H * C57BL/6 * C57BL/6N	normal nervous system phenotype	J:232167
Fustm1c(EUCOMM)Wtsi/Fustm1c(EUCOMM)Wtsi involves: C3H * C57BL/6 * C57BL/6N	no abnormal phenotype detected	J:232167
Fustm1d(EUCOMM)Wtsi/Fustm1d(EUCOMM)Wtsi involves: 129S4/SvJae * C3H * C57BL/6 * C57BL/6J * C57BL/6N	neonatal lethality, complete penetrance	J:232167