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Phenotypes Associated with This Genotype
Genotype
MGI:5426937
Allelic
Composition
Wlstm1Xzg/Wlstm1Xzg
Tg(Msx2-cre)5Rem/0
Genetic
Background
Not Specified
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(Msx2-cre)5Rem mutation (2 available)
Wlstm1Xzg mutation (0 available); any Wls mutation (36 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
limbs/digits/tail
• dorsally flexed
• contains reduced and malformed muscle mass at E17.5
• dorsally flexed
• impaired patterning; more severe in the ventral limb than in dorsal limb
• at E10.5, mesenchymal cells exhibit decreased proliferation while apoptosis is increased in the distal limb mesenchyme compared with wild-type cells
• mice exhibit dysgenesis of limb soft tissue with progressive defects from proximal to distal compared with wild-type mice
• thin and narrow at E10.5
• more severe in hindlimbs than forelimbs

embryo
• thin and narrow at E10.5

cellular
• of distal limb mesenchyme cells at E12.5
• of limb mesenchyme cells at E12.5

skeleton
• in the forelimbs at E17.5
• in the forelimbs at E17.5

integument
• limb hair follicle formation is blocked
• limb dermis differentiation is blocked

muscle
• in the forelimbs at E17.5
• impaired in the autopod
• in the forelimbs at E17.5


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
03/18/2025
MGI 6.24
The Jackson Laboratory