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Phenotypes Associated with This Genotype
Genotype
MGI:3769002
Allelic
Composition
Fgf3tm1.1Sms/Fgf3tm1.1Sms
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fgf3tm1.1Sms mutation (0 available); any Fgf3 mutation (16 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• at weaning, only 9% of heterozygous intercross offspring were homozygous mutant, indicating significant lethality associated with this allele

limbs/digits/tail

hearing/vestibular/ear
• showed only rudimentary partitioning into distended cochlear chamber
• showed only rudimentary partitioning into distended vestibular chamber
• the swollen cochlear duct showed incomplete partition and poor coiling
• absence or severe truncation of the anterior and posterior semicircular canals in some
• absence or severe truncation of the anterior and posterior semicircular canals in some
• all affected mutant ears had a distended membranous labyrinth
• fusion of utricle and saccule
• fusion of utricle and saccule
• significantly elevated ABR thresholds in one or both ears

behavior/neurological
• a light head tilt were seen in mice showing significant ABR threshold increase only in one ear
• in mice showing significant ABR threshold increase in bilateral ears


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