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Phenotypes Associated with This Genotype
Genotype
MGI:5660194
Allelic
Composition
Mapk1tm1Gela/Mapk1tm1Gela
H2az2Tg(Wnt1-cre)11Rth/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
H2az2Tg(Wnt1-cre)11Rth mutation (2 available); any H2az2 mutation (25 available)
Mapk1tm1Gela mutation (1 available); any Mapk1 mutation (34 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• although present in late gestation, no viable neonates are detected

craniofacial

cardiovascular system
• in 1 of 5 mice at E16.5
• in 1 of 4 mice at E17.5
• in 2 of 5 mice at E16.5

endocrine/exocrine glands
• in 1 of 5 mice at E16.5
• in 1 of 5 mice at E16.5

growth/size/body

digestive/alimentary system

immune system
• in 1 of 5 mice at E16.5

hematopoietic system
• in 1 of 5 mice at E16.5

skeleton

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
velocardiofacial syndrome DOID:12583 OMIM:192430
J:144862


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
01/31/2023
MGI 6.22
The Jackson Laboratory