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Phenotypes Associated with This Genotype
Genotype
MGI:3639857
Allelic
Composition
Neurog2tm1Fgu/Neurog2tm1Fgu
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Neurog2tm1Fgu mutation (0 available); any Neurog2 mutation (18 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• most mutants die during the first postnatal day
• mutants surviving past the first day die between 4 and 25 days of age

growth/size/body
• homozygotes are smaller in size than littermates
• mutants surviving past the first day exhibit progressive growth retardation until time of death

behavior/neurological
• mutants are unable to feed normally, as their stomachs lacked milk and were filled with air
• mutants exhibit abnormal limb posturing
• mutants exhibit a low level of activity after birth
• surviving mutants exhibit decreased motor activity with time until death between 4 and 25 days of age

nervous system
• at 13.5 all parasympathetic ganglia of the head are missing
• visceromotor neurons project abnormally in the facial nerve
• in E10.5 embryos a subtle increase in the number of dI3 and dI5 neurons is seen
• but, no significant changes in the number of dI2 and dI4/6 neurons is detected
• neuronal differentiation is absent or abnormal in this ganglion
• neuronal differentiation is absent or abnormal in this ganglion
• neither the corda tympani nor the greater superficial petrosal nerve have formed at E11.5
• mice show a transient defect in neurogenesis in populations of sensory neurons in the DRGs


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
04/30/2024
MGI 6.23
The Jackson Laboratory