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Phenotypes Associated with This Genotype
Genotype
MGI:3584506
Allelic
Composition
Foxp2tm1Bux/Foxp2tm1Bux
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Foxp2tm1Bux mutation (0 available); any Foxp2 mutation (52 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Histological analysis of brains of Foxp2tm1Bux and wild type mice

mortality/aging
• homozygotes typically die by 21 days of age; however, maternal care of homozygotes and feeding appear normal

behavior/neurological
• mean righting during a fall is reduced
• righting response is delayed
• decreased spontaneous activity
• at 6 days of age the incidence of vocalization over time is reduced and at 10 days of age a profound decrease in ultrasonic vocalizations and the incidence of clicks is observed; however the duration, peak frequency, and bandwidth of the vocalizations are normal

nervous system
• gaps are seen in the glial network while in some areas glial fibers appear clumped
• a 3 - 4 cell thick external granule cell layer is seen at 15 - 17 days of age; however increased apoptosis is not seen in this layer
• Purkinje cells frequently fail to align in a continuous row, often forming a layer that is several cells thick with ectopic ells in the granule cell layer
• the dendritic arbors are less elaborate and often aligned at oblique angles
• the molecular layer is about half the thickness of wild-type

growth/size/body

hearing/vestibular/ear

vision/eye

craniofacial

cellular
• gaps are seen in the glial network while in some areas glial fibers appear clumped


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