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Phenotypes Associated with This Genotype
Genotype
MGI:4421038
Allelic
Composition
Dmrt3tm1Hgc/Dmrt3tm1Hgc
Genetic
Background
Not Specified
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dmrt3tm1Hgc mutation (0 available); any Dmrt3 mutation (12 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• death by starvation at around 2 months of age

behavior/neurological
N
• motor coordination and balance were largely normal in mutant mice
• mutant mice, but not control mice (wild-type littermates), had major difficulties running at higher velocities on a treadmill
• limb coordination in neonatal mice, scored during air-stepping, was markedly different
• mutant mice spent less time swimming
• showed frequent twitching limb movements rarely observed in controls
• swing times (flexion) were increased in all limbs, whereas stance time (extension) was increased in forelimbs
• alternating hindlimb movements were almost absent in mutant mice
• mutant mice may emphasize extension movements, resulting in a longer stride
• significantly increased stride length in all limbs of mutant mice

craniofacial

nervous system
• decreases in spinal commissural interneuron numbers in mutant mice compared to wild-type at E15
• 58% increase in the number of Wt1+ spinal cord neurons in mutant mice
• analysis of central pattern generator output in the isolated neonatal spinal cord using drug-induced fictive locomotion shows that cords from mutant mice have uncoordinated and irregular firing rhythms as well as increased burst and interburst durations compared to control animals

reproductive system
• abnormalities in male sexual development

skeleton

growth/size/body


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
04/16/2024
MGI 6.23
The Jackson Laboratory