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Phenotypes Associated with This Genotype
Genotype
MGI:3838794
Allelic
Composition
Pou4f2tm4(DTA)Whk/Pou4f2tm4(DTA)Whk
Tg(Six3-cre)69Frty/?
Genetic
Background
involves: 129S/SvEv * C57BL/6 * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pou4f2tm4(DTA)Whk mutation (1 available); any Pou4f2 mutation (7 available)
Tg(Six3-cre)69Frty mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• clearly abnormal in 16 day old mice
• thinner with smaller diameter fibers
• unmyelinated fibers
• deformed at E14.5
• overall structure remains normal through 5 months of age
• reduced cell proliferation and increased apoptosis
• more than 98% of retinal ganglion cells ablated at E14.5
• only displaced amacrine cells present at 16 days of age
• noticeably thinner at E14.5
• 30-50% thinner than controls at 16 days of age
• saturated amplitudes of both light and dark adapted b-waves 25% of normal
• dark adapted a-wave amplitude 42% of normal
• negative scotopic threshold response is very small
• positive scotopic threshold response is absent

nervous system
• clearly abnormal in 16 day old mice
• thinner with smaller diameter fibers
• unmyelinated fibers
• deformed at E14.5


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
05/14/2024
MGI 6.23
The Jackson Laboratory