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Phenotypes Associated with This Genotype
Genotype
MGI:5315491
Allelic
Composition
Ror1tm1.1Meg/Ror1tm1.1Meg
Ror2tm1.1Meg/Ror2tm1.1Meg
H2az2Tg(Wnt1-cre)11Rth/H2az2+
Genetic
Background
involves: 129S4/SvJae * 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)
Ror1tm1.1Meg mutation (1 available); any Ror1 mutation (58 available)
Ror2tm1.1Meg mutation (1 available); any Ror2 mutation (124 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Ror1tm1.1Meg/Ror1tm1.1Meg Ror2tm1.1Meg/Ror2tm1.1Meg H2az2Tg(Wnt1-cre)11Rth/0 embryos exhibit sympathetic axon branching defects

nervous system
• sympathetic innervation defects are seen in several target organs at E17.5
• defects are similar to those in Wnt5a null mice
• however, sympathetic chain ganglia appear grossly intact


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
01/06/2026
MGI 6.24
The Jackson Laboratory