51 phenotypes from 5 alleles in 6 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Criptotm1Eda/Criptotm1Eda either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6)	abnormal gastrulation	J:186907
	abnormal mesoderm development	J:186907
	abnormal primitive streak formation	J:186907
	embryonic growth arrest	J:186907
Criptotm1Eda/Criptotm1Eda either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * Black Swiss) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	abnormal amnion morphology	J:51595
	abnormal cell adhesion	J:51595
	abnormal chorion morphology	J:51595
	abnormal developmental patterning	J:51595
	abnormal embryonic neuroepithelium morphology	J:51595
	abnormal embryonic tissue morphology	J:51595
	abnormal extraembryonic tissue morphology	J:51595
	abnormal heart development	J:51595
	abnormal mesoderm development	J:51595
	abnormal rostral-caudal axis patterning	J:51595
	abnormal visceral yolk sac blood island morphology	J:51595
	absent somites	J:51595
	absent vitelline blood vessels	J:51595
	decreased fibroblast proliferation	J:51595
	normal embryo phenotype	J:51595
	embryonic lethality, complete penetrance	J:51595
	short rostral-caudal axis	J:51595
Criptotm1Mms/Criptotm1Mms either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss)	abnormal embryonic neuroepithelium morphology	J:50343
	abnormal gastrulation	J:50343
	abnormal germ layer development	J:50343
	abnormal heart development	J:50343
	abnormal mesoderm development	J:50343
	abnormal rostral-caudal axis patterning	J:50343
	abnormal visceral endoderm morphology	J:50343
	absent mesoderm	J:50343
	absent somites	J:50343
	embryonic lethality during organogenesis, complete penetrance	J:50343
	failure of primitive streak formation	J:50343
Criptotm1Mms/Criptotm2Mms involves: 129S6/SvEvTac * C57BL/6	abnormal endoderm development	J:104418
	abnormal mesendoderm development	J:104418
	absent anterior definitive endoderm	J:104418
	absent notochord	J:104418
	absent prechordal plate	J:104418
	cyclopia	J:104418
	decreased forebrain size	J:104418
	decreased midbrain size	J:104418
	fused somites	J:104418
	holoprosencephaly	J:104418
	premature death	J:104418
	rostral body truncation	J:104418
Criptotm2.2Mms/Criptotm2.2Mms involves: 129S6/SvEvTac * FVB/N	no abnormal phenotype detected	J:104418
Criptotm2Mms/Criptotm2.1Mms involves: 129S6/SvEvTac * C57BL/6	abnormal endoderm development	J:104418
	abnormal mesendoderm development	J:104418
	absent anterior definitive endoderm	J:104418
	absent notochord	J:104418
	absent prechordal plate	J:104418
	cyclopia	J:104418
	decreased forebrain size	J:104418
	decreased midbrain size	J:104418
	fused somites	J:104418
	holoprosencephaly	J:104418
	premature death	J:104418
	rostral body truncation	J:104418
Pgrtm2(cre)Lyd/Pgr+ Criptotm2.2Mms/Criptotm2.2Mms involves: 129/Sv * C57BL/6N * CD-1	abnormal decidualization	J:324146
	abnormal embryo attachment	J:324146
	abnormal endometrial gland morphology	J:324146
	abnormal luminal closure	J:324146
	abnormal pregnancy	J:324146
	abnormal uterine environment	J:324146
	abnormal uterine-embryonic axis	J:324146
	decreased litter size	J:324146
	delayed embryo implantation	J:324146
	endometrium inflammation	J:324146
	failure of embryo implantation	J:324146
	female infertility	J:324146
	reduced female fertility	J:324146