83 phenotypes from 7 alleles in 16 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
PorcnGt(CSD256)Byg/Y chimera involves: 129P2/OlaHsd	abnormal digit morphology	J:186934
	abnormal embryonic tissue morphology	J:160967
	abnormal vas deferens morphology	J:186934
	abnormal ventral body wall morphology	J:186934
	alopecia	J:186934
	dermal cyst	J:186934
	fused phalanges	J:186934
	hydronephrosis	J:186934
	infertility	J:186934
	prenatal lethality	J:186934
	skin lesions	J:186934
	thin epidermis	J:186934
	true hermaphroditism	J:186934
Porcntm1.1Jrt/Y B6.Cg-Porcntm1.1Jrt	no abnormal phenotype detected	J:198636
Porcntm1.1Jrt/Porcn+ B6.Cg-Porcntm1.1Jrt	no abnormal phenotype detected	J:198636
Porcntm1.1Jrt/Y involves: 129S6/SvEvTac * C57BL/6NCr * ICR	no abnormal phenotype detected	J:198636
Porcntm1.1Jrt/Porcn+ involves: 129S6/SvEvTac * C57BL/6NCr * ICR	no abnormal phenotype detected	J:198636
Porcntm1.1Jrt/Porcn+ Tg(CAG-EGFP)D4Nagy/0 Tg(Zp3-cre)3Mrt/0 involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6J * C57BL/6NCr * FVB/N	normal embryo phenotype	J:198636
Porcntm1.1Jrt/Porcn+ Tg(CAG-cre)1Nagy/0 involves: 129S6/SvEvTac * C57BL/6NCr * ICR	abnormal allantois morphology	J:198636
	abnormal embryo development	J:198636
	abnormal placenta morphology	J:198636
	abnormal umbilical cord morphology	J:198636
	normal embryo phenotype	J:198636
	embryonic lethality during organogenesis, complete penetrance	J:198636
	normal nervous system phenotype	J:198636
Porcntm1.1Jrt/Porcn+ Tg(Ttr-cre)1Hadj/0 involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NCr * CBA/J	normal mortality/aging	J:198636
Porcntm1.1Jrt/Y Tg(CAG-cre)1Nagy/0 involves: 129S6/SvEvTac * C57BL/6NCr * ICR	abnormal extraembryonic tissue morphology	J:198636
	absent amnion	J:198636
	absent chorion	J:198636
	decreased embryo size	J:198636
	embryonic lethality between implantation and somite formation, complete penetrance	J:198636
Porcntm1.1Jrt/Y Tg(CAG-EGFP)D4Nagy/0 Tg(Zp3-cre)3Mrt/0 involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6J * C57BL/6NCr * FVB/N	failure to gastrulate	J:198636
Porcntm1.1Lcm/Y involves: 129S1/Sv * 129X1/SvJ * C57BL/6	no abnormal phenotype detected	J:173672
Porcntm1.1Lcm/Porcn+ H2az2Tg(Wnt1-cre)11Rth/H2az2+ Tg(rx3-icre)1Mjam/0 involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J * CD-1	abnormal retina pigmentation	J:218165
	coloboma	J:218165
	microphthalmia	J:218165
Porcntm1.1Lcm/Porcn+ Edil3Tg(Sox2-cre)1Amc/Edil3+ involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	abnormal autopod morphology	J:173672
	abnormal hair follicle development	J:173672
	abnormal tail morphology	J:173672
	absent ulna	J:173672
	caudal body truncation	J:173672
	cleft palate	J:173672
	decreased body size	J:173672
	hairless	J:173672
	normal integument phenotype	J:173672
	omphalocele	J:173672
	perinatal lethality, complete penetrance	J:173672
	short tail	J:173672
	sternum hypoplasia	J:173672
	thin dermal layer	J:173672
Porcntm1.1Lcm/Y Edil3Tg(Sox2-cre)1Amc/Edil3+ involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	abnormal mesoderm development	J:173672
	lethality throughout fetal growth and development, complete penetrance	J:173672
Porcntm1.1Lcm/Y H2az2Tg(Wnt1-cre)11Rth/H2az2+ involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J * CD-1	abnormal craniofacial development	J:218165
	abnormal craniofacial morphology	J:218165
	abnormal midbrain-hindbrain boundary morphology	J:218165
	cleft palate	J:218165
	coloboma	J:218165
	midline cleft upper lip	J:218165
Porcntm1.1Lcm/Y H2az2Tg(Wnt1-cre)11Rth/H2az2+ Tg(rx3-icre)1Mjam/0 involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J * CD-1	abnormal anterior eye segment morphology	J:218165
	abnormal craniofacial morphology	J:218165
	abnormal midbrain-hindbrain boundary morphology	J:218165
	abnormal retina pigmentation	J:218165
	cleft palate	J:218165
	coloboma	J:218165
	decreased cornea thickness	J:218165
	failure of eyelid fusion	J:218165
	iris hypoplasia	J:218165
	midline cleft upper lip	J:218165
Porcntm1.1Lcm/Porcntm1.1Lcm involves: 129S1/Sv * 129X1/SvJ * C57BL/6	no abnormal phenotype detected	J:173672
Porcntm1.1Lcm/Porcntm1.2Lcm involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1	abnormal craniofacial morphology	J:218165
	abnormal midbrain-hindbrain boundary morphology	J:218165
	abnormal retina pigmentation	J:218165
	coloboma	J:218165
	failure of eyelid fusion	J:218165
Porcntm1.1Lcm/Porcntm1.2Lcm Tg(Six3-cre)69Frty/0 involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * DBA/2	abnormal craniofacial morphology	J:218165
	abnormal midbrain-hindbrain boundary morphology	J:218165
	abnormal retina pigmentation	J:218165
	coloboma	J:218165
	failure of eyelid fusion	J:218165
	failure of ventral body wall closure	J:218165
	skin hypoplasia	J:218165
Porcntm1.1Lcm/Y Tg(Msx2-cre)5Rem/0 involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal dermal layer morphology	J:173672
	abnormal skin morphology	J:173672
	decreased autopod size	J:173672
	syndactyly	J:173672
Porcntm1.1Lcm/Y Tg(Prrx1-cre)1Cjt/0 involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL/J	oligodactyly	J:173672
	short limbs	J:173672
Porcntm1.1Lcm/Y Tg(rx3-icre)1Mjam/0 involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1	abnormal craniofacial morphology	J:218165
	abnormal midbrain-hindbrain boundary morphology	J:218165
	abnormal retina pigmentation	J:218165
	coloboma	J:218165
Porcntm1.1Vdv/Porcn+ Tg(KRT14-cre)1Efu/0 involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6J	abnormal hair growth	J:186934
Porcntm1.1Vdv/Porcn+ Tg(EIIa-cre)C5379Lmgd/0 involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6J * FVB/N	abnormal hair growth	J:186934
	prenatal lethality, incomplete penetrance	J:186934
Porcntm1.1Vdv/Porcn+ Hprt1tm1(CAG-cre)Mnn/Hprt1+ involves: 129S/Sv * C57BL/6J	abnormal ventral body wall morphology	J:186934
	caudal body truncation	J:186934
	embryonic growth retardation	J:186934
	embryonic lethality during organogenesis, incomplete penetrance	J:186934
	open neural tube	J:186934
	prenatal lethality, complete penetrance	J:186934
Porcntm1.1Vdv/Y Tg(EIIa-cre)C5379Lmgd/0 involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6J * FVB/N	abnormal hair growth	J:186934
	prenatal lethality, incomplete penetrance	J:186934
Porcntm1.1Vdv/Y Tg(KRT14-cre)1Efu/0 involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6J	abnormal hair follicle development	J:186934
	abnormal hypodermis fat layer morphology	J:186934
	abnormal tooth morphology	J:186934
	alopecia	J:186934
	thin skin	J:186934
Porcntm1.1Vdv/Y Tg(Prrx1-cre)1Cjt/0 involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6 * SJL/J	brachydactyly	J:186934
	decreased body size	J:186934
	decreased length of long bones	J:186934
	postnatal growth retardation	J:186934
	short limbs	J:186934
	syndactyly	J:186934
Porcntm1.2Lcm/Porcntm1.2Lcm involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * DBA/2	abnormal craniofacial morphology	J:218165
	abnormal limb morphology	J:218165
	abnormal midbrain-hindbrain boundary morphology	J:218165
	abnormal retina pigmentation	J:218165
	caudal body truncation	J:218165
	coloboma	J:218165
	curly tail	J:218165
	failure of eyelid fusion	J:218165
	forelimb oligodactyly	J:218165
	short tail	J:218165
	syndactyly	J:218165
Porcntm1.2Vdv/Porcn+ involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6J * FVB/N	abnormal hair growth	J:186934
	embryonic lethality, incomplete penetrance	J:186934
	prenatal lethality, incomplete penetrance	J:186934
Porcntm1.2Vdv/Y involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6J * FVB/N	embryonic lethality, complete penetrance	J:186934
Porcntm1Vdv/Porcn+ chimera involves: 129S5/SvEvBrd * C57BL/6J	abnormal caudal vertebrae morphology	J:186934
	abnormal uterine horn morphology	J:186934
	brachydactyly	J:186934
	fused phalanges	J:186934
	hydronephrosis	J:186934
	oligodactyly	J:186934
Porcntm1Vdv/Y chimera involves: 129S5/SvEvBrd * C57BL/6J	abnormal caudal vertebrae morphology	J:186934
	brachydactyly	J:186934
	fused phalanges	J:186934
	hydronephrosis	J:186934
	oligodactyly	J:186934
	small testis	J:186934