54 phenotypes from 5 alleles in 8 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Ctnna1em1Xjz/Ctnna1em1Xjz C57BL/6J-Ctnna1em1Xjz	prenatal lethality, complete penetrance	J:328283
Ctnna1Gt(fVET3A)Hiir/Ctnna1Gt(fVET3A)Hiir involves: C3H * C57BL/6	absent blastocoele	J:224530
Ctnna1Gt(pGT1.8geo)4Pgr/Ctnna1Gt(pGT1.8geo)4Pgr involves: 129S1/Sv * 129X1/SvJ	abnormal embryonic tissue morphology	J:38208
	abnormal extraembryonic tissue morphology	J:38208
	absent blastocoele	J:38208
	absent inner cell mass	J:38208
	embryonic lethality before implantation, complete penetrance	J:38208
Ctnna1tm1Efu/Ctnna1tm1Efu involves: 129X1/SvJ	abnormal skin physiology	J:144091
Ctnna1tm1Efu/Ctnna1tm1Efu A1cfTg(Myh6-cre/Esr1*)1Jmk/A1cf+ involves: 129X1/SvJ * FVB/N	dilated cardiomyopathy	J:197814
Ctnna1tm1Efu/Ctnna1tm1Efu Tg(KRT14-cre)1Efu/? involves: 129X1/SvJ	abnormal cell adhesion	J:67797
	abnormal dermal layer morphology	J:67797
	abnormal epidermal layer morphology	J:67797
	abnormal epidermis stratum basale morphology	J:67797
	abnormal hair follicle development	J:67797
	abnormal keratinocyte morphology	J:67797
	abnormal limb development	J:67797
	absent vibrissae	J:67797
	epidermal desquamation	J:67797
	increased keratinocyte proliferation	J:67797
	pointed snout	J:67797
	thick epidermis	J:67797
	thick epidermis stratum basale	J:67797
Ctnna1tm1Efu/Ctnna1tm1Efu Tg(MMTV-cre)4Mam/? involves: 129X1/SvJ * FVB	abnormal hair follicle development	J:87469
	abnormal mammary gland epithelium morphology	J:87469
	abnormal mammary gland epithelium physiology	J:87469
	abnormal milk composition	J:87469
	increased mammary gland apoptosis	J:87469
Ctnna1tm1Efu/Ctnna1tm1Efu Tg(Nes-cre)1Kln/? involves: 129X1/SvJ * C57BL/6 * SJL	abnormal brain development	J:106707
	abnormal brain morphology	J:106707
	abnormal lateral ventricle morphology	J:106707
	abnormal mitosis	J:106707
	abnormal neuron differentiation	J:106707
	increased brain weight	J:106707
	megacephaly	J:106707
	postnatal growth retardation	J:106707
	postnatal lethality, complete penetrance	J:106707
	thickened cerebral cortex	J:106707
Ctnna1tm1Efu/Ctnna1tm1Efu Tg(Wap-cre)11738Mam/? involves: 129X1/SvJ * C57BL/6 * SJL	abnormal mammary gland epithelium morphology	J:87469
	abnormal milk composition	J:87469
	decreased body weight	J:87469
	increased mammary gland apoptosis	J:87469
	maternal effect	J:87469
	postnatal growth retardation	J:87469
Ctnna1tm1Efu/Ctnna1tm1Efu Twist2tm1(cre)Dor/Twist2+ involves: 129X1/SvJ	abnormal skeleton development	J:178499
	decreased width of hypertrophic chondrocyte zone	J:178499
	delayed intramembranous bone ossification	J:178499
Ctnna1Tvrm5/Ctnna1+ C57BL/6J-Ctnna1Tvrm5/Pjn	abnormal c-wave shape	J:227177
	abnormal eye electrophysiology	J:227177
	abnormal retina pigment epithelium morphology	J:227177
	abnormal retina pigmentation	J:227177
	abnormal rod electrophysiology	J:227177
Ctnna1Tvrm5/Ctnna1Tvrm5 C57BL/6J-Ctnna1Tvrm5/Pjn	abnormal c-wave shape	J:227177
	abnormal eye electrophysiology	J:227177
	abnormal ocular fundus morphology	J:227177
	abnormal retina outer limiting membrane morphology	J:227177
	abnormal retina pigment epithelium morphology	J:227177
	abnormal retina pigmentation	J:227177
	abnormal rod electrophysiology	J:227177
	decreased a-wave amplitude	J:227177
	decreased b-wave amplitude	J:227177
	retina cone cell degeneration	J:227177
	retina photoreceptor degeneration	J:227177
	retina rod cell degeneration	J:227177
	retina spots	J:227177
	thin retina outer nuclear layer	J:227177