69 phenotypes from 9 alleles in 15 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Cdx2tm1.1Aral/Cdx2tm1.1Aral Tg(Zp3-cre)93Knw/0 involves: 129X1/SvJ * C57BL/6 * CD-1 * SJL	normal reproductive system phenotype	J:189005
Cdx2tm1.1Aral/Cdx2tm1.2Aral Tg(Zp3-cre)93Knw/0 involves: 129X1/SvJ * C57BL/6 * CD-1 * SJL	normal reproductive system phenotype	J:189005
Cdx2tm1.1Aral/Cdx2tm1Fbe Tg(Zp3-cre)93Knw/0 involves: 129X1/SvJ * C57BL/6 * CD-1 * SJL	embryonic growth arrest	J:189005
	embryonic lethality before implantation, complete penetrance	J:189005
Cdx2tm1.1Lhn/Cdx2+ Tg(CAG-cre/ERT2)F34Fmr/0 involves: 129S1/Sv * 129X1/SvJ * CD-1	absent tail	J:154904
	short tail	J:154904
	sirenomelia	J:154904
Cdx2tm1.1Lhn/Cdx2tm1.1Lhn Tg(CAG-cre/ERT2)F34Fmr/0 involves: 129S1/Sv * 129X1/SvJ * CD-1	abnormal mesoderm development	J:154904
	abnormal presomitic mesoderm morphology	J:154904
	absent hindlimb buds	J:154904
	decreased somite size	J:154904
	embryonic lethality during organogenesis, complete penetrance	J:154904
	impaired somite development	J:154904
	short rostral-caudal axis	J:154904
Cdx2tm1.2Aral/Cdx2tm1Fbe involves: 129X1/SvJ * C57BL/6 * CD-1 * SJL	embryonic growth arrest	J:189005
	embryonic lethality before implantation, complete penetrance	J:189005
Cdx2tm1Fbe/Cdx2+ involves: 129S1/Sv * C57BL/6 * CBA	abnormal placenta labyrinth morphology	J:104372
	failure of chorioallantoic fusion	J:104372
Cdx2tm1Fbe/Cdx2+ involves: 129S1/Sv * C57BL/6J	abnormal rib morphology	J:38772
	cervical vertebral transformation	J:38772
	decreased body weight	J:38772
	increased colon adenoma incidence	J:38772
	increased intestinal adenoma incidence	J:38772
	kinked tail	J:38772
	short tail	J:38772
	thoracic vertebral transformation	J:38772
	vertebral transformation	J:38772
Cdx2tm1Fbe/Cdx2tm1Fbe involves: 129S1/Sv * C57BL/6J	embryonic lethality, complete penetrance	J:38772
	failure of embryo implantation	J:38772
Cdx2tm1Fbe/Cdx2tm1Fbe involves: ICR	abnormal blastocoele morphology	J:98502
	abnormal blastocyst morphology	J:98502
	abnormal inner cell mass apoptosis	J:98502
	abnormal trophectoderm morphology	J:98502
	abnormal trophoblast layer morphology	J:98502
	absent trophoblast giant cells	J:98502
	embryonic lethality before implantation, complete penetrance	J:98502
	failure of blastocyst to hatch from the zona pellucida	J:98502
	increased trophectoderm apoptosis	J:98502
Cdx2tm1Fbe/Cdx2tm2.1Fbe involves: 129P2/OlaHsd * 129S1/Sv * BALB/cJ	caudal body truncation	J:179732
Cdx2tm1Fbe/Cdx2tm2Fbe Edil3Tg(Sox2-cre)1Amc/Edil3+ involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6 * CBA	caudal body truncation	J:179732
Cdx2tm1Khk/Cdx2tm1Khk involves: C57BL/6 * SJL	no abnormal phenotype detected	J:149479
Cdx2tm1Khk/Cdx2tm1Khk Tg(Foxa3-cre)1Khk/0 involves: C57BL/6 * DBA * SJL	abnormal cecum morphology	J:149479
	abnormal digestive system development	J:149479
	abnormal duodenum morphology	J:149479
	abnormal enteroendocrine cell morphology	J:149479
	abnormal hindgut morphology	J:149479
	abnormal intestinal epithelium morphology	J:149479
	abnormal intestinal goblet cell morphology	J:149479
	abnormal intestine morphology	J:149479
	absent colon	J:149479
	absent enterocytes	J:149479
	decreased small intestinal villus size	J:149479
	distended duodenum	J:149479
	neonatal lethality, complete penetrance	J:149479
Cdx2tm1Mmt/Cdx2+ B6.129X1-Cdx2tm1Mmt	abnormal cell cycle checkpoint function	J:86737
	abnormal chromosome morphology	J:86737
	abnormal colon morphology	J:86737
	abnormal small intestine morphology	J:86737
	decreased apoptosis	J:86737
	increased apoptosis	J:86737
Cdx2tm1Mmt/Cdx2+ involves: 129X1/SvJ * C57BL/6	abnormal cecum morphology	J:47050
	abnormal colon morphology	J:47050
	abnormal rib morphology	J:47050
	colon polyps	J:47050
	decreased body size	J:47050
	increased colon hamartoma incidence	J:47050
	vertebral transformation	J:47050
Cdx2tm1Mmt/Cdx2tm1Mmt involves: 129X1/SvJ * C57BL/6	absent inner cell mass proliferation	J:47050
	embryonic lethality between implantation and somite formation, complete penetrance	J:47050
Cdx2tm1Yxz/Cdx2tm1Yxz involves: 129S4/SvJae * C57BL/6 * CD-1	no abnormal phenotype detected	J:186304
Cdx2tm2.1Fbe/Cdx2+ involves: 129P2/OlaHsd * BALB/cJ	intestine polyps	J:179732
Cdx2tm2Fbe/Cdx2tm2Fbe Lgr5tm1(cre/ERT2)Cle/Lgr5+ involves: 129P2/OlaHsd * C57BL/6	abnormal cell migration	J:179732
	abnormal crypts of Lieberkuhn morphology	J:179732
	abnormal intestine physiology	J:179732
	abnormal Paneth cell physiology	J:179732
	increased Paneth cell number	J:179732
Cdx2tm2Fbe/Cdx2tm2Fbe Tg(Cyp1a1-cre/ERT)1Dwi/0 involves: 129P2/OlaHsd * C57BL/6 * CBA	abnormal cell migration	J:179732
	abnormal crypts of Lieberkuhn morphology	J:179732
	abnormal ileum morphology	J:179732
	abnormal intestinal mucosa morphology	J:179732
	abnormal intestine physiology	J:179732
	abnormal Paneth cell physiology	J:179732
	abnormal small intestinal villus morphology	J:179732
	cecum polyps	J:179732
	increased Paneth cell number	J:179732