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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Inpp5etm1.2Ssch
targeted mutation 1.2, Stephane Schurmans
MGI:4360187
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Inpp5etm1.2Ssch/Inpp5etm1.2Ssch involves: 129S1/Sv * 129X1/SvJ MGI:4360188
cn2
Inpp5etm1.1Ssch/Inpp5etm1.2Ssch
Tg(CAG-cre/Esr1*)5Amc/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA MGI:4360189


Genotype
MGI:4360188
hm1
Allelic
Composition
Inpp5etm1.2Ssch/Inpp5etm1.2Ssch
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Inpp5etm1.2Ssch mutation (0 available); any Inpp5e mutation (29 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• fewer than expected embryos are found at E18.5 (14.8% vs 25% expected)
• mice die soon after birth
• fewer than expected embryos are found at E13.5 (16.9% vs 25% expected)

vision/eye
• eye development stops at the optic vesicle stage prior to the appearance of the optic cup
• all show bilateral anophthalmia

renal/urinary system
• in cystic tubules primary cilia are sparse and appear dilated
• cilia in noncystic tubules appear normal
• about 2% of glomeruli are cystic
• seen in all mice
• cysts originate in the cortical collecting and connecting ducts, the proximal tubules and the descending limb of the loop of Henle
• only rarely are the glomeruli cystic
• in cystic glomeruli cilia in Bowman's capsule appear abnormal

cellular
• serum starved ciliated MEFs stimulated by growth factor signaling tend to lose their cilia and remaining cilia appear short and dilated, unlike similarly treated control MEFs
• in cystic tubules primary cilia are sparse and appear dilated
• cilia in noncystic tubules appear normal

limbs/digits/tail
• delayed ossification
• over 60% show postaxial hexadactyly
• delayed ossification

craniofacial
• seen in 75% of mice

digestive/alimentary system
• seen in 75% of mice

skeleton
• delayed ossification
• delayed ossification
• seen in 50% of mice
• delayed ossification of the metacarpals and phalanges

nervous system
• cerebral developmental defects, including anencephaly, are seen in 30% of mice at E15.5
• cerebral developmental defects, including exencephaly, are seen in 30% of mice at E15.5

growth/size/body
• seen in 75% of mice
• about 2% of glomeruli are cystic
• seen in all mice
• cysts originate in the cortical collecting and connecting ducts, the proximal tubules and the descending limb of the loop of Henle
• only rarely are the glomeruli cystic




Genotype
MGI:4360189
cn2
Allelic
Composition
Inpp5etm1.1Ssch/Inpp5etm1.2Ssch
Tg(CAG-cre/Esr1*)5Amc/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Inpp5etm1.1Ssch mutation (0 available); any Inpp5e mutation (29 available)
Inpp5etm1.2Ssch mutation (0 available); any Inpp5e mutation (29 available)
Tg(CAG-cre/Esr1*)5Amc mutation (9 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• mice display increased body weight after tamoxifen treatment
• glomerular cysts are seen in 6 month old tamoxifen treated mice

renal/urinary system
• glomerular cysts are seen in 6 month old tamoxifen treated mice

vision/eye
• after tamoxifen treatment the retinal photoreceptor layer is completely absent





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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory