49 phenotypes from 6 alleles in 9 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Bptfem1(IMPC)Bay/Bptf+ C57BL/6N-Bptfem1(IMPC)Bay/Bay	abnormal bone structure	J:211773
	decreased body length	J:211773
	decreased prepulse inhibition	J:211773
	vertebral fusion	J:211773
Bptfem1(IMPC)Bay/Bptfem1(IMPC)Bay C57BL/6N-Bptfem1(IMPC)Bay/Bay	preweaning lethality, complete penetrance	J:211773
Bptfem1Zfa/Bptfem1Zfa Lgr5tm1(cre/ERT2)Cle/Lgr5+ involves: 129P2/OlaHsd * C57BL/6	abnormal digestive system development	J:268724
Bptfem1Zfa/Bptfem1Zfa Tg(Rorc-cre)1Litt/0 involves: C57BL/6 * FVB	decreased common lymphocyte progenitor cell number	J:259392
	increased susceptibility to bacterial infection	J:259392
	increased susceptibility to bacterial infection induced morbidity/mortality	J:259392
BptfGt(A012C04)Wrst/BptfGt(A012C04)Wrst either: 129S2/SvPas-BptfGt(A012C04)Wrst or B6.129S2-BptfGt(A012C04)Wrst or (involves: 129S2/SvPas * CD-1)	abnormal chorion morphology	J:142592
	abnormal developmental patterning	J:142592
	abnormal egg cylinder morphology	J:142592
	abnormal extraembryonic tissue morphology	J:142592
	abnormal primitive streak elongation	J:142592
	abnormal primitive streak formation	J:142592
	abnormal proximal-distal axis patterning	J:142592
	abnormal rostral-caudal axis patterning	J:142592
	abnormal visceral endoderm morphology	J:142592
	absent chorion	J:142592
	decreased embryo size	J:142592
	embryonic growth arrest	J:142592
	embryonic growth retardation	J:142592
	embryonic lethality during organogenesis, complete penetrance	J:142592
	small ectoplacental cone	J:142592
	thick embryonic epiblast	J:142592
BptfGt(XG023)Byg/BptfGt(XG023)Byg involves: 129P2/OlaHsd	abnormal rostral-caudal axis patterning	J:147414
	absent anterior visceral endoderm	J:147414
	absent distal visceral endoderm	J:147414
	absent mesoderm	J:147414
	decreased cell proliferation	J:147414
	embryonic growth arrest	J:147414
	embryonic lethality between implantation and somite formation, complete penetrance	J:147414
	failure of primitive streak formation	J:147414
BptfGt(XG023)Byg/Bptftm1.2Cwu involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	embryonic growth arrest	J:147414
	embryonic lethality between implantation and somite formation, complete penetrance	J:147414
Bptftm1.1Cwu/Bptftm1.1Cwu Emx1tm1(cre)Krj/Emx1+ involves: 129S1/Sv * 129S2/SvPas * C57BL/6	abnormal cerebral cortex morphology	J:334252
	abnormal head shape	J:334252
	abnormal neuron specification	J:334252
	abnormal neuronal precursor proliferation	J:334252
	abnormal stratification in cerebral cortex	J:334252
	normal behavior/neurological phenotype	J:334252
	decreased body weight	J:334252
	decreased brain weight	J:334252
	decreased forebrain size	J:334252
	decreased neuronal precursor cell number	J:334252
	forebrain hypoplasia	J:334252
	increased neuron apoptosis	J:334252
	microgliosis	J:334252
	normal mortality/aging	J:334252
Bptftm1.1Cwu/Bptftm1.1Cwu Foxg1tm1(cre)Skm/? involves: 129P2/OlaHsd-Hprtb-m3 * 129S1/Sv-Oca2+ Tyr+ Kitl+	abnormal olfactory sensory neuron morphology	J:217534
	perinatal lethality, complete penetrance	J:217534
Bptftm1.2Cwu/Bptftm1.2Cwu involves: 129S1/Sv * C57BL/6	abnormal ectoderm development	J:147414
	abnormal endoderm development	J:147414
	absent mesoderm	J:147414
	decreased embryo size	J:147414
	embryonic lethality between implantation and somite formation, complete penetrance	J:147414