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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(Kera-cre)KC4.3Wwk
transgene insertion KC4.3, Winston W Y Kao
MGI:3849605
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Col5a1tm2.1Rjw/Col5a1tm2.1Rjw
Tg(Kera-cre)KC4.3Wwk/0
involves: 129 * C57BL/6 * FVB/N * SJL MGI:5661552
cn2
Tg(CAG-cat,-Dcn*)#Debi/0
Tg(Kera-cre)KC4.3Wwk/0
involves: FVB/N MGI:5298094


Genotype
MGI:5661552
cn1
Allelic
Composition
Col5a1tm2.1Rjw/Col5a1tm2.1Rjw
Tg(Kera-cre)KC4.3Wwk/0
Genetic
Background
involves: 129 * C57BL/6 * FVB/N * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Col5a1tm2.1Rjw mutation (0 available); any Col5a1 mutation (66 available)
Tg(Kera-cre)KC4.3Wwk mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• adult mice display abnormal fibril structure and stromal disorganization
• larger and less uniform collagen fibrils are seen throughout the cornea stroma, with disrupted fibril packing
• a significant decrease in fibril density and inter-fibril space is noted in both anterior and posterior regions of the stroma
• adult mice exhibit a 14% decrease in corneal stroma thickness relative to wild-type controls
• in the anterior stroma, the mean stromal fibril diameter increased to 42.5+/-12.8 nm versus 25.3+/-3.4 nm in control corneas
• the range of anterior stroma fibril diameters is 8-95 nm versus 14-42 nm in control corneas
• a 58% decrease in the number of fibrils per unit area is noted in the anterior stroma
• in the posterior stroma, the mean stromal fibril diameter increased to 34.7+/-6.7 nm versus 27.5+/-3.3 nm in control corneas
• the range of posterior stroma fibril diameters is 12-61 nm versus 14-39 nm in control corneas
• a 36% decrease in the number of fibrils per unit area is noted in the posterior stroma
• at P30 and P90, mice exhibit a heterogeneous collagen fibril population containing fibrils with very large diameters
• structurally abnormal fibrils with irregular profiles are commonly observed
• the fibril phenotype shows an anterior-posterior difference, with the anterior stroma containing larger and more heterogeneous fibrils than the posterior stroma
• a significant decrease in fibril density is noted in both anterior and posterior regions of the stroma
• adult mice exhibit conspicuous corneal stromal opacity
• at P60, backscattered light is observed throughout the corneal stroma, with more haze in the anterior stroma
• mice exhibit a 3.5-fold increase in the average light scattering per micrometer thickness of the corneal stroma relative to wild-type controls

growth/size/body
N
• mice are viable and fertile with no significant differences in body weight at P10 or P30 relative to wild-type controls




Genotype
MGI:5298094
cn2
Allelic
Composition
Tg(CAG-cat,-Dcn*)#Debi/0
Tg(Kera-cre)KC4.3Wwk/0
Genetic
Background
involves: FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
No mouse lines available in IMSR.
See publication links below for author information.
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• lamellar structure is disrupted, more severely in the posterior stroma
• relatively normal lamellae are separated by abnormal zones in which collagen fibrils are irregularly packed and embedded in an electron lucent substance
• collagen fibrillogenesis is altered, interfibril spacing is increased, and in electron lucent zones fibril diameters are reduced
• disruption of the lamellar structure is more severe in the posterior stroma
• the extent of stromal opacity varies from hardly visualized cloudiness to overt opacity
• generally develop by about 1 month of age with a slow progression of opacity afterward
• opacity is more severe in the central cornea

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
congenital stromal corneal dystrophy DOID:0060445 OMIM:610048
J:177392





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last database update
04/09/2024
MGI 6.23
The Jackson Laboratory