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Phenotypes Associated with This Genotype
Genotype
MGI:3604385
Allelic
Composition
Wnt3atm1Amc/Wnt3avt
Genetic
Background
involves: 129S1/Sv * C3H/HeJ * C57BL/6J * C57BR
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Wnt3atm1Amc mutation (1 available); any Wnt3a mutation (29 available)
Wnt3avt mutation (1 available); any Wnt3a mutation (29 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• only about 50% of compound heterozygotes live longer than 4 weeks compared to 90% of Wnt3avt heterozygotes

limbs/digits/tail

skeleton
• deformities seen as far anterior as the 7th thoracic vertebra
• the most severely affected mutants have a reduction in the number of thoracic vertebrae
• none of the compound heterozygotes have all of the lumbar vertebrae
• no normal sacral vertebrae are seen

embryo
• the most severely affected mutants are smaller than wild-type littermates
• the most severely affected mutants display spina bifida of the posterior neural tube
• somites do not extend as far caudally as in wild-type embryos and malformed somites are seen rostral to the last somite

nervous system
• the most severely affected mutants display spina bifida of the posterior neural tube

behavior/neurological
• the most severely affected mutants display hindlimb paralysis

growth/size/body
• the most severely affected mutants are smaller than wild-type littermates

renal/urinary system
• in several cases severely affected mutants displayed accumulation of urine in the kidneys and ureters

digestive/alimentary system
• in several cases severely affected mutants displayed hyperextended intestines


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
03/31/2026
MGI 6.24
The Jackson Laboratory