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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Foxp2+
wild type
MGI:2441314
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
ht1
Foxp2tm1Momo/Foxp2+ involves: 129S6/SvEvTac * C57BL/6 MGI:3789850
ht2
Foxp2R552H/Foxp2+ involves: BALB/c * C3H/HeH MGI:3795716
ht3
Foxp2tm1Bux/Foxp2+ involves: C57BL/6 MGI:3584507
ht4
Foxp2tm2.2Woen/Foxp2+ involves: C57BL/6 * C57BL/6J MGI:3851148


Genotype
MGI:3789850
ht1
Allelic
Composition
Foxp2tm1Momo/Foxp2+
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Foxp2tm1Momo mutation (2 available); any Foxp2 mutation (52 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Motor and ultrasonic vocalization impairment in Foxp2tm1Momo/Foxp2tm1Momo and Foxp2tm1Momo/Foxp2+ mice

behavior/neurological
• at P10, heterozygous pups show a modest impairment of ultrasonic vocalization when separated from mothers
• heterozygous pups produce three vocalizations, including whistle-type vocalizations similar to wild-type vocalizations, as well as short-length and click-type sonic vocalizations that are not normally seen in wild-type

growth/size/body
• homozygotes show a 10-15% reduction in weight by P10




Genotype
MGI:3795716
ht2
Allelic
Composition
Foxp2R552H/Foxp2+
Genetic
Background
involves: BALB/c * C3H/HeH
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Foxp2R552H mutation (0 available); any Foxp2 mutation (52 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system

behavior/neurological
• motor skill learning on a running wheel is impaired compared to wild-type mice




Genotype
MGI:3584507
ht3
Allelic
Composition
Foxp2tm1Bux/Foxp2+
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

behavior/neurological
• 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 is observed; however the duration, peak frequency, and bandwidth of the vocalizations are normal

nervous system
• radial glial fibers appear less well aligned and thinner
• a 1 cell thick external granule cell layer is seen at 15 - 17 days of age; however adult heterozygotes lack an external granule cell layer similar to wild-type mice

growth/size/body

cellular
• radial glial fibers appear less well aligned and thinner




Genotype
MGI:3851148
ht4
Allelic
Composition
Foxp2tm2.2Woen/Foxp2+
Genetic
Background
involves: C57BL/6 * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Foxp2tm2.2Woen mutation (0 available); any Foxp2 mutation (52 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• on a modified hole board
• increased exploration of a novel object
• mice react less to a clicking sound than wild-type mice
• mice exhibit slightly impaired motor learning on a rotarod compared with wild-type mice

homeostasis/metabolism
• mice exhibit lower plasma inorganic phosphorus levels compared with wild-type mice
• mice exhibit a slightly higher plasma Ferritin levels compared with wild-type mice
• in the frontal cortex, cerebellum, caudate-putamen, nucleus accumbens, and globus pallidus
• mice assimilate more energy than wild-type mice
• increased in the frontal cortex, cerebellum, caudate-putamen, nucleus accumbens, and globus pallidus

respiratory system
• mice exhibit higher respiratory rate during activity and at rest compared with wild-type mice

immune system

adipose tissue

cardiovascular system
• mice exhibit a lower pulse rate than wild-type mice

growth/size/body

hematopoietic system





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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
03/18/2025
MGI 6.24
The Jackson Laboratory