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Phenotypes Associated with This Genotype
Genotype
MGI:4943549
Allelic
Composition
Tdrd7nmf166/Tdrd7nmf166
Genetic
Background
involves: C3H * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tdrd7nmf166 mutation (1 available); any Tdrd7 mutation (43 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• posterior uveitis in 2 mice at 0ver 24 months of age
• severe optic nerve atrophy characterized by retinal ganglion cell axon loss and excavative remodeling of the optic nerve are seen
• iris flattening is detected by 4 months of age
• increased depth is seen by 4 months of age
• lens extrusion at later stages
• in some cases the mass of fiber cells pass through the pupil into the anterior chamber of the eye
• rupture and extrusion of fiber cell mass into the vitreous at later stages
• develop vacuoles at later stages
• all develop posterior cataracts by 4 weeks of age that become more severe with age
• detected in some mice by 6 months of age
• incidence increases with age

reproductive system
• arrests at the round spermatid stage

nervous system
• severe optic nerve atrophy characterized by retinal ganglion cell axon loss and excavative remodeling of the optic nerve are seen

immune system
• posterior uveitis in 2 mice at 0ver 24 months of age


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
04/16/2024
MGI 6.23
The Jackson Laboratory