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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Cpoxnct
Nakano cataract
MGI:1856966
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Cpoxnct/Cpoxnct involves: BALB/cCrSlc MGI:5488915
hm2
Cpoxnct/Cpoxnct Not Specified MGI:4399726
cx3
Cpoxnct/Cpoxnct
Nctm1BALB/c/Nctm1BALB/c
involves: BALB/c * MSM MGI:3036070
cx4
Cpoxnct/Cpoxnct
Nctm2BALB/c/Nctm2BALB/c
involves: BALB/c * MSM MGI:3036071


Genotype
MGI:5488915
hm1
Allelic
Composition
Cpoxnct/Cpoxnct
Genetic
Background
involves: BALB/cCrSlc
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cpoxnct mutation (1 available); any Cpox mutation (33 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• at 10 weeks
• however, mice also expression a transgene containing the endogenous gene do not develop cataracts during the 6 month observation period

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
hereditary coproporphyria DOID:13269 OMIM:121300
J:196645




Genotype
MGI:4399726
hm2
Allelic
Composition
Cpoxnct/Cpoxnct
Genetic
Background
Not Specified
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cpoxnct mutation (1 available); any Cpox mutation (33 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• histological analysis shows slower than normal loss of lens cell nuclei, especially in the bow area, by 7 days of age (J:5481)
• persistence of cell nuclei in the bow area is noteable at 12-13 days of age (J:5481)
• there is a decrease in crystallin and leakage of crystallin from the lens (J:6014)
• distal portions of many fibers swell and become hydropic
• at 20-23 days of age lens fibers are disintegrating posterior to the center of the lens with histology showing broken cell borders, many vacuoles and large swollen cells
• an opaque spot first appears in mutant mice between 16 to 22 days of age
• the whole lens is opaque by 4-5 weeks of age




Genotype
MGI:3036070
cx3
Allelic
Composition
Cpoxnct/Cpoxnct
Nctm1BALB/c/Nctm1BALB/c
Genetic
Background
involves: BALB/c * MSM
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cpoxnct mutation (1 available); any Cpox mutation (33 available)
Nctm1BALB/c mutation (0 available); any Nctm1 mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• decreased cataract severity




Genotype
MGI:3036071
cx4
Allelic
Composition
Cpoxnct/Cpoxnct
Nctm2BALB/c/Nctm2BALB/c
Genetic
Background
involves: BALB/c * MSM
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cpoxnct mutation (1 available); any Cpox mutation (33 available)
Nctm2BALB/c mutation (0 available); any Nctm2 mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• decreased cataract severity





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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory