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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
H3c14Aey69
abnormal eyes 69
MGI:6342045
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
cx1
Gja8Aey69/Gja8Aey69
H3c14Aey69/H3c14Aey69
C3HeB/FeJ MGI:6342121


Genotype
MGI:6342121
cx1
Allelic
Composition
Gja8Aey69/Gja8Aey69
H3c14Aey69/H3c14Aey69
Genetic
Background
C3HeB/FeJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gja8Aey69 mutation (1 available); any Gja8 mutation (33 available)
H3c14Aey69 mutation (1 available); any H3c14 mutation (7 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• failure of detachment of transient connection between surface ectoderm (future cornea) and lens vesicle at age E13.5
• lens vesicle filled with pycnotic and disorganized cells at age E13.5
• small and disorganized lens vesicle starting in embryos age E11.5
• normal formation of lens vesicle in embryos age E10.5
• abnormal bending of retinal layers anterior to cornea at age E17.5
• retinal pigmented epithelium (RPE) covering entire anterior part of eye at age P1
• establishment of outer and inner neuroblastic layers in neural retina
• thicker and larger retina at age E17.5
• post-partum invasion of central part of the eye (filling up lens and vitreous space) by RPE and other retinal layers

embryo
N
• viable

growth/size/body

homeostasis/metabolism
• reduced blood lipid levels (hypolipidemia)

reproductive system

behavior/neurological
• increased rearing
• increased locomotor activity





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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
05/07/2024
MGI 6.23
The Jackson Laboratory