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Phenotypes Associated with This Genotype
Genotype
MGI:6368185
Allelic
Composition
Porcntm1.1Lcm/Y
H2az2Tg(Wnt1-cre)11Rth/H2az2+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J * CD-1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
H2az2Tg(Wnt1-cre)11Rth mutation (2 available); any H2az2 mutation (26 available)
Porcntm1.1Lcm mutation (0 available); any Porcn mutation (18 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
craniofacial
• abnormal development of facial primordia
• a mild, fully penetrant median cleft lip

vision/eye
• in some mice

nervous system

growth/size/body
• a mild, fully penetrant median cleft lip

digestive/alimentary system

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
focal dermal hypoplasia DOID:2120 OMIM:305600
J:218165


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory