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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Sox10tm5Weg
targeted mutation 5, Michael Wegner
MGI:3723291
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Sox10tm5Weg/Sox10tm5Weg involves: 129P2/OlaHsd * C3H MGI:3759669
ht2
Sox10tm5Weg/Sox10+ involves: 129P2/OlaHsd * C3H MGI:3759671


Genotype
MGI:3759669
hm1
Allelic
Composition
Sox10tm5Weg/Sox10tm5Weg
Genetic
Background
involves: 129P2/OlaHsd * C3H
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Sox10tm5Weg mutation (0 available); any Sox10 mutation (33 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• all mice are born alive but die within a few hours after birth

nervous system
N
• unlike mice homozygous for Sox10tm1Weg, cranial and sympathetic ganglia morphology are similar to wild-type
• stomach wall contains a fully developed enteric nervous system (ENS) at E18.5 in contrast to the complete lack of ENS in Sox10tm1Weg
• few enteric neural crest, neurons or glia cells are detected in small or large intestine
• colonization of the intestines by enteric nervous system cells is variable but never goes beyond the duodenum
• the number of myelinating oligodendrocytes is reduced to about 65% of wild-type levels
• expression analysis indicates that Schwann cells fail to mature to the myelinating stage by E18.5
• levels of apoptosis in glia and neuronal cells are increased at E14.5 embryos while expression on the mutant protein is decrease
• severe reduction in size at E18.5
• however, unlike mice homozygous for Sox10tm1Weg ganglia morphology is similar to wild-type at E10.5 and E11.5

embryo
• the number of migrating melanoblasts near the eye of E12.5 embryos are reduced
• number of melanoblasts in E12.5 embryos in the hindlimb region is 20% of that found in wild-type

cellular
• the number of migrating melanoblasts near the eye of E12.5 embryos are reduced
• number of melanoblasts in E12.5 embryos in the hindlimb region is 20% of that found in wild-type




Genotype
MGI:3759671
ht2
Allelic
Composition
Sox10tm5Weg/Sox10+
Genetic
Background
involves: 129P2/OlaHsd * C3H
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Sox10tm5Weg mutation (0 available); any Sox10 mutation (33 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype
• unlike mice heterozygous for some other Sox10 alleles, mice do not develop megacolon or belly spots





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last database update
05/07/2024
MGI 6.23
The Jackson Laboratory