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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Ppcd1
posterior polymorphous corneal dystrophy 1
MGI:4830871
Summary 8 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Ppcd1/Ppcd1 D2.129-Ppcd1 MGI:5912182
ht2
Ppcd1/+ D2.129-Ppcd1 MGI:4830893
ht3
Ppcd1/+ (D2.129-Ppcd1 x C57BL/6)F1 MGI:4830890
ht4
Ppcd1/+ (D2.129-Ppcd1 x FVB/N)F1 MGI:4830891
ht5
Ppcd1/+ involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:4830892
cx6
Kat14tm1a(KOMP)Wtsi/Ppcd1 D2.Cg-Kat14tm1a(KOMP)Wtsi/Ppcd1 MGI:5912187
cx7
Kat14tm1d(KOMP)Wtsi/Ppcd1 D2.Cg-Kat14tm1d(KOMP)Wtsi/Ppcd1 MGI:5912185
cx8
Dzank1tm1a(KOMP)Wtsi/Ppcd1 involves: 129S1/Sv * 129X1/SvJ * C57BL/6N * DBA/2J MGI:5912189


Genotype
MGI:5912182
hm1
Allelic
Composition
Ppcd1/Ppcd1
Genetic
Background
D2.129-Ppcd1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ppcd1 mutation (1 available); any Ppcd1 mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• no live pups are recovered




Genotype
MGI:4830893
ht2
Allelic
Composition
Ppcd1/+
Genetic
Background
D2.129-Ppcd1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ppcd1 mutation (1 available); any Ppcd1 mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Eye abnormalities in Ppcd1/0 mice

vision/eye
• at P3, the cells in the iridocorneal angle are more densely packed than in wild-type mice
• at P5, the iridocorneal angle is occluded compared to in wild-type mice
• however, the irridocorneal angle is normal immediately after birth
• the trabecular meshwork of the eye is occluded by multilayered, stratified endothelial cells that exhibit an epithelial morphology, are visible in the iridocorneal angle and on the posterior surface of the cornea and anterior surface of the iris, and migrate onto the central cornea unlike in wild-type mice
• mice exhibit inappropriate cytokeratin AE1/AE3 immunoreactivity in the corneal endothelium and iridocorneal angle, extending onto the anterior surface of the iris and posterior surface of the cornea unlike in wild-type mice
• mice exhibit lens subluxation and proliferation of cells over the surface of the lens unlike wild-type mice
• eye diameter is increased compared to in wild-type mice

cardiovascular system




Genotype
MGI:4830890
ht3
Allelic
Composition
Ppcd1/+
Genetic
Background
(D2.129-Ppcd1 x C57BL/6)F1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ppcd1 mutation (1 available); any Ppcd1 mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• Background Sensitivity: 38% of mice exhibit enlarged eyes in an F1 cross to C57BL/6 compared with 44% of mice in F1 cross to FVB/N




Genotype
MGI:4830891
ht4
Allelic
Composition
Ppcd1/+
Genetic
Background
(D2.129-Ppcd1 x FVB/N)F1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ppcd1 mutation (1 available); any Ppcd1 mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• Background Sensitivity: 44% of mice exhibit enlarged eyes in an F1 cross to FVB/N compared with 38% of mice in an F1 cross to C57BL/6




Genotype
MGI:4830892
ht5
Allelic
Composition
Ppcd1/+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ppcd1 mutation (1 available); any Ppcd1 mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Eye abnormalities in Ppcd1/0 mice

vision/eye
N
• mice backcrossed to C57BL/6 for 3 generations do not exhibit the Corneal Dystrophy, Posterior Polymorphous, 1 (PPCD1) phenotype
• mice exhibit corneal haze, neovascularization, ulcers, and scarring unlike wild-type mice
• the anterior chamber is deep and enlarged compared to in wild-type mice
• mice exhibit lens subluxation unlike wild-type mice

cardiovascular system




Genotype
MGI:5912187
cx6
Allelic
Composition
Kat14tm1a(KOMP)Wtsi/Ppcd1
Genetic
Background
D2.Cg-Kat14tm1a(KOMP)Wtsi/Ppcd1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Kat14tm1a(KOMP)Wtsi mutation (3 available); any Kat14 mutation (75 available)
Ppcd1 mutation (1 available); any Ppcd1 mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• no mice are present when survival is scored at weaning




Genotype
MGI:5912185
cx7
Allelic
Composition
Kat14tm1d(KOMP)Wtsi/Ppcd1
Genetic
Background
D2.Cg-Kat14tm1d(KOMP)Wtsi/Ppcd1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Kat14tm1d(KOMP)Wtsi mutation (0 available); any Kat14 mutation (75 available)
Ppcd1 mutation (1 available); any Ppcd1 mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• no mice are present when survival is scored at weaning




Genotype
MGI:5912189
cx8
Allelic
Composition
Dzank1tm1a(KOMP)Wtsi/Ppcd1
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6N * DBA/2J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dzank1tm1a(KOMP)Wtsi mutation (1 available); any Dzank1 mutation (43 available)
Ppcd1 mutation (1 available); any Ppcd1 mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• 50% of mice die prior to birth





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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory