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Phenotypes Associated with This Genotype
Genotype
MGI:3663922
Allelic
Composition
Fevtm1Esd/Fevtm1Esd
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fevtm1Esd mutation (0 available); any Fev mutation (14 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• small number of deaths within the first week of life

nervous system
• serotonin neuron development disrupted in the hindbrain
• precursors formed but most fail to differentiate
• 70% loss of serotinin immunoreactive cell bodies in adult brains
• greatly diminished density of serotonin immunoreactive neurons in the cortex and hippocampus
• B nuclei of the hind brain are missing

behavior/neurological
• shorter latency to attack
• although locomotor activity is normal, mice spend less than normal time in the central areas during an open field test
• never enter the open arms in a plus maze test
• initial rotarod performance poor in comparison to controls
• later performance becomes comparable to controls

cellular
• serotonin neuron development disrupted in the hindbrain
• precursors formed but most fail to differentiate
• 70% loss of serotinin immunoreactive cell bodies in adult brains
• greatly diminished density of serotonin immunoreactive neurons in the cortex and hippocampus
• B nuclei of the hind brain are missing


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