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Phenotypes Associated with This Genotype
Genotype
MGI:3693850
Allelic
Composition
Fgf2tm1Zllr/Fgf2tm1Zllr
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fgf2tm1Zllr mutation (0 available); any Fgf2 mutation (17 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• in newborn homozygotes, a fraction of neuronal progenitors fail to colonize their target cortical layers III and II during cerebral cortex development; as a result, a greater number (~17%) of BrdU-labeled cells remain in the deeper cortical layers (VI-IV) and the corpus callosum relative to wild-type mice (~8.8%)
• this defect is variable, as many more BrdU-positive cells (25-36%) are found in the corpus callosum and deep layers of severely affected homozygotes, whereas a few others are indistinguishable from wild-type
• adult homozygotes display varying degrees of ectopic parvalbumin-positive neurons in the hippocampal commissure
• adult homozygotes display varying degrees of ectopic parvalbumin-positive neurons in the hippocampal commissure located beneath the cerebral cortex
• at birth, homozygotes show defects in organization and differentiation of the cerebral cortex
• at birth, only a few differentiated, large pyramidal neurons are detected in the cerebral cortex
• at birth, all differentiating cortical layers appear compressed and less distinct
• an average reduction of ~25% in parvalbumin-positive neurons is observed in all cortical layers
• however, no differences in the distribution of astroglial cells are observed
• no significant differences are noted in cell survival in either embryonic (E16), newborn or adult cerebral cortex, as shown by TUNEL analysis
• at birth, the thickness of the cerebral cortex is reduced by ~10%
• adult homozygotes show neuronal abnormalities throughout the mantle layer of the cervical spinal cord, with only a few differentiated large neurons while all other neural cell types appear normal
• adult homozygotes respond normally to chronic angiotensin II infusion but show an impaired baroreceptor reflex
• in response to an acute vasodilatory stimulus (isoproterenol), all homozygotes, but no wild-type mice, display a significant drop in blood pressure along with an impaired increase in heart rates, indicating autonomic dysfunction

cardiovascular system
• on average, the blood pressure of adult homozygotes is reduced by ~10 mmHg relative to wild-type littermates
• however, no differences in baseline plasma renin values, heart rates or body weights are observed

behavior/neurological
N
• homozygotes do NOT develop seizures or reeler-like phenotypes

hearing/vestibular/ear
N
• homozygotes exhibit normal inner ear morphogenesis with no detectable abnormalities at the adult stage
• in addition, homozygotes show no significant differences in hearing thresholds before and after noise-induced cochlear damage relative to wild-type littermates

cellular
• in newborn homozygotes, a fraction of neuronal progenitors fail to colonize their target cortical layers III and II during cerebral cortex development; as a result, a greater number (~17%) of BrdU-labeled cells remain in the deeper cortical layers (VI-IV) and the corpus callosum relative to wild-type mice (~8.8%)
• this defect is variable, as many more BrdU-positive cells (25-36%) are found in the corpus callosum and deep layers of severely affected homozygotes, whereas a few others are indistinguishable from wild-type
• adult homozygotes display varying degrees of ectopic parvalbumin-positive neurons in the hippocampal commissure


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
04/09/2024
MGI 6.23
The Jackson Laboratory