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Phenotypes Associated with This Genotype
Genotype
MGI:5518647
Allelic
Composition
Sox11tm1.1Gan/Sox11tm1.1Gan
Tg(Six3-cre)69Frty/0
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Sox11tm1.1Gan mutation (0 available); any Sox11 mutation (14 available)
Tg(Six3-cre)69Frty mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Decrease in retinal ganglion cells in single Sox11tm1.1Gan and Sox4tm1Vlf homozygous conditional mutants and abolishment of retinal ganglion cells in Sox11tm1.1Gan/Sox11tm1.1Gan Sox4tm1Vlf/Sox4tm1Vlf Tg(Six3-cre)69Frty/0 retinas

vision/eye
N
• mice exhibit normal numbers of horizontal, Muller glial, cone and rod cells
• 2-fold increase starting at E14.5
• impaired retinal ganglion cell development
• reduced number of axon bundles in the retina
• in the inner nuclear layer and ganglion cell layer
• beginning from E12.5 to E16.5
• moderate at P0 and in adult mice

growth/size/body
• moderate
• however, mice exhibit normal body weight and size by P30

cellular
• 2-fold increase starting at E14.5
• reduced in retinal axon bundles

nervous system
• reduced in retinal axon bundles
• in the inner nuclear layer and ganglion cell layer
• beginning from E12.5 to E16.5
• moderate at P0 and in adult mice


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
03/25/2025
MGI 6.24
The Jackson Laboratory