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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Grhl3tm3.1Jane
targeted mutation 3.1, Stephen M Jane
MGI:5306651
Summary 6 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Grhl3tm3.1Jane/Grhl3tm3.1Jane involves: 129S1/Sv * C57BL/6 MGI:5306658
cn2
Grhl1tm1Jane/Grhl1tm1Jane
Grhl3tm1Jane/Grhl3tm3.1Jane
Tg(KRT14-cre/ERT)20Efu/0
involves: 129S1/Sv * C57BL/6 * CD-1 MGI:5896360
cn3
Grhl3tm1Jane/Grhl3tm3.1Jane
Tg(MMTV-cre)4Mam/0
involves: 129S1/Sv * C57BL/6 * FVB MGI:5306660
cn4
Grhl3tm1Jane/Grhl3tm3.1Jane
Tg(KRT14-cre)8Brn/0
involves: 129S1/Sv * C57BL/6 * FVB/N MGI:5306659
cn5
Grhl1tm1Jane/Grhl1tm1Jane
Grhl3tm1Jane/Grhl3tm3.1Jane
Tg(KRT14-cre)8Brn/0
involves: 129S1/Sv * C57BL/6 * FVB/N MGI:5896359
cn6
Grhl3tm1Jane/Grhl3tm3.1Jane
Tgm5tm2a(KOMP)Wtsi/Tgm5tm2a(KOMP)Wtsi
Tg(KRT14-cre)8Brn/0
involves: 129S1/Sv * C57BL/6N * FVB/N MGI:5896358


Genotype
MGI:5306658
hm1
Allelic
Composition
Grhl3tm3.1Jane/Grhl3tm3.1Jane
Genetic
Background
involves: 129S1/Sv * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Grhl3tm3.1Jane mutation (1 available); any Grhl3 mutation (53 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype
• mice are healthy and fertile




Genotype
MGI:5896360
cn2
Allelic
Composition
Grhl1tm1Jane/Grhl1tm1Jane
Grhl3tm1Jane/Grhl3tm3.1Jane
Tg(KRT14-cre/ERT)20Efu/0
Genetic
Background
involves: 129S1/Sv * C57BL/6 * CD-1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Grhl1tm1Jane mutation (1 available); any Grhl1 mutation (33 available)
Grhl3tm1Jane mutation (1 available); any Grhl3 mutation (53 available)
Grhl3tm3.1Jane mutation (1 available); any Grhl3 mutation (53 available)
Tg(KRT14-cre/ERT)20Efu mutation (3 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• all die within 7 weeks of tamoxifen treatment

integument
• regression of skin barrier function after tamoxifen treatment
• dye penetration is variegated matching the pattern of cre mediated gene deletion
• after tamoxifen treatment gross abnormalities and increased fragility are seen
• after tamoxifen treatment

homeostasis/metabolism
• regression of skin barrier function after tamoxifen treatment
• dye penetration is variegated matching the pattern of cre mediated gene deletion




Genotype
MGI:5306660
cn3
Allelic
Composition
Grhl3tm1Jane/Grhl3tm3.1Jane
Tg(MMTV-cre)4Mam/0
Genetic
Background
involves: 129S1/Sv * C57BL/6 * FVB
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Grhl3tm1Jane mutation (1 available); any Grhl3 mutation (53 available)
Grhl3tm3.1Jane mutation (1 available); any Grhl3 mutation (53 available)
Tg(MMTV-cre)4Mam mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
integument
• authors state that mice exhibit a phenotype identical to Grhl3tm1Jane/Grhl3tm3.1Jane Tg(KRT14-cre)8Brn mice
• authors state that mice exhibit a phenotype identical to Grhl3tm1Jane/Grhl3tm3.1Jane Tg(KRT14-cre)8Brn mice

neoplasm
• authors state that mice exhibit a phenotype identical to Grhl3tm1Jane/Grhl3tm3.1Jane Tg(KRT14-cre)8Brn mice




Genotype
MGI:5306659
cn4
Allelic
Composition
Grhl3tm1Jane/Grhl3tm3.1Jane
Tg(KRT14-cre)8Brn/0
Genetic
Background
involves: 129S1/Sv * C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Grhl3tm1Jane mutation (1 available); any Grhl3 mutation (53 available)
Grhl3tm3.1Jane mutation (1 available); any Grhl3 mutation (53 available)
Tg(KRT14-cre)8Brn mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
integument
N
• from E18.5 through 8 weeks, mice exhibit normal skin barrier formation (J:178952)
• no overt skin barrier defect or abnormality of the cornified envelope of the stratum corneum from birth to 6 weeks of age (J:233531)
• in aged mice
• spontaneously in aged mice affecting the snout and neck
• in 4 weeks after DMBA/TPA treatment
• spontaneously in aged mice affecting the snout and neck
• in 4 weeks after DMBA/TPA treatment

neoplasm
• 4 weeks after DMBA/TPA treatment, mice develop skin papillomas many which progress to squamous cell carcinomas unlike control mice
• spontaneously in aged mice affecting the snout and neck
• in 4 weeks after DMBA/TPA treatment
• spontaneously in aged mice affecting the snout and neck
• in 4 weeks after DMBA/TPA treatment

homeostasis/metabolism
• 4 weeks after DMBA/TPA treatment, mice develop skin papillomas many which progress to squamous cell carcinomas unlike control mice




Genotype
MGI:5896359
cn5
Allelic
Composition
Grhl1tm1Jane/Grhl1tm1Jane
Grhl3tm1Jane/Grhl3tm3.1Jane
Tg(KRT14-cre)8Brn/0
Genetic
Background
involves: 129S1/Sv * C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Grhl1tm1Jane mutation (1 available); any Grhl1 mutation (33 available)
Grhl3tm1Jane mutation (1 available); any Grhl3 mutation (53 available)
Grhl3tm3.1Jane mutation (1 available); any Grhl3 mutation (53 available)
Tg(KRT14-cre)8Brn mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• present in expected numbers at E18.5 but all died by P3 with most lost during the first 48 hours after birth

integument
• at P2 excessive fluid loss and regression of skin barrier function leads to dehydration and death
• loss of cornified envelope integrity by P2

homeostasis/metabolism
• at P2 excessive fluid loss and regression of skin barrier function leads to dehydration and death




Genotype
MGI:5896358
cn6
Allelic
Composition
Grhl3tm1Jane/Grhl3tm3.1Jane
Tgm5tm2a(KOMP)Wtsi/Tgm5tm2a(KOMP)Wtsi
Tg(KRT14-cre)8Brn/0
Genetic
Background
involves: 129S1/Sv * C57BL/6N * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Grhl3tm1Jane mutation (1 available); any Grhl3 mutation (53 available)
Grhl3tm3.1Jane mutation (1 available); any Grhl3 mutation (53 available)
Tg(KRT14-cre)8Brn mutation (4 available)
Tgm5tm2a(KOMP)Wtsi mutation (1 available); any Tgm5 mutation (35 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
N
• present in expected numbers at E18.5 and 6 weeks of age

integument
N
• no evidence of skin barrier dysfunction was seen





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last database update
10/09/2024
MGI 6.24
The Jackson Laboratory