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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Krt1tm1Tmm
targeted mutation 1, Thomas M Magin
MGI:5495252
Summary 6 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Krt1tm1Tmm/Krt1tm1Tmm involves: 129 * C57BL/6 MGI:5495259
cx2
Krt1tm1Tmm/Krt1+
Krt10tm2Tmm/Krt10tm2Tmm
involves: 129P2/OlaHsd * BALB/c * C57BL/6 MGI:5495261
cx3
Krt1tm1Tmm/Krt1tm1Tmm
Krt10tm2Tmm/Krt10+
involves: 129P2/OlaHsd * BALB/c * C57BL/6 MGI:5495262
cx4
Krt1tm1Tmm/Krt1tm1Tmm
Krt10tm2Tmm/Krt10tm2Tmm
involves: 129P2/OlaHsd * BALB/c * C57BL/6 MGI:5495260
cx5
Krt1tm1Tmm/Krt1tm1Tmm
S100a9tm1Nck/S100a9tm1Nck
involves: 129P2/OlaHsd * C57BL/6 MGI:5509366
cx6
Il18tm1Khe/Il18tm1Khe
Krt1tm1Tmm/Krt1tm1Tmm
involves: 129P2/OlaHsd * C57BL/6 MGI:5509364


Genotype
MGI:5495259
hm1
Allelic
Composition
Krt1tm1Tmm/Krt1tm1Tmm
Genetic
Background
involves: 129 * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Krt1tm1Tmm mutation (0 available); any Krt1 mutation (68 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

integument
• 2-fold increase in trans-epidermal water loss
• however, outside-in epidermal barrier is normal
• mild skin defect
• reduced number of intact cornified envelopes
• however, treatment with IL18-blocking antibodies rescues number of intact cornified envelopes

immune system
• increased IL33 in the serum of newborn mice
• in newborn mice but not epidermal extracts
• increased IL33 in epidermal extracts

cardiovascular system
• increased vascularization at the dermal/epidermal interface indicated by increased PECAM staining
• leaky capillary in the lungs at P0

growth/size/body
• mild postnatally

homeostasis/metabolism
• increased IL33 in the serum of newborn mice
• in newborn mice but not epidermal extracts
• 2-fold increase in trans-epidermal water loss
• however, outside-in epidermal barrier is normal

nervous system

hematopoietic system




Genotype
MGI:5495261
cx2
Allelic
Composition
Krt1tm1Tmm/Krt1+
Krt10tm2Tmm/Krt10tm2Tmm
Genetic
Background
involves: 129P2/OlaHsd * BALB/c * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Krt10tm2Tmm mutation (1 available); any Krt10 mutation (32 available)
Krt1tm1Tmm mutation (0 available); any Krt1 mutation (68 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice die within the first hours after birth due to generalized multiple small and some extended lesions caused by mechanical load

integument
• fragile skin upon mechanical load
• however, the water barrier remains intact




Genotype
MGI:5495262
cx3
Allelic
Composition
Krt1tm1Tmm/Krt1tm1Tmm
Krt10tm2Tmm/Krt10+
Genetic
Background
involves: 129P2/OlaHsd * BALB/c * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Krt10tm2Tmm mutation (1 available); any Krt10 mutation (32 available)
Krt1tm1Tmm mutation (0 available); any Krt1 mutation (68 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice die within the first hours after birth due to generalized multiple small and some extended lesions caused by mechanical load

integument
• fragile skin upon mechanical load
• however, the water barrier remains intact




Genotype
MGI:5495260
cx4
Allelic
Composition
Krt1tm1Tmm/Krt1tm1Tmm
Krt10tm2Tmm/Krt10tm2Tmm
Genetic
Background
involves: 129P2/OlaHsd * BALB/c * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Krt10tm2Tmm mutation (1 available); any Krt10 mutation (32 available)
Krt1tm1Tmm mutation (0 available); any Krt1 mutation (68 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice die within the first hours after birth due to generalized multiple small and some extended lesions caused by mechanical load

integument
• smaller desmosomes at E18.5 in the upper epidermis than in wild-type mice
• some are misshapen with inclusions or empty appearance
• thick and disorganized with impaired cornified envelop differentiation
• devoid of intermediate filaments
• flattened keratinocytes
• premature degradation of nuclei in suprabasal epidermis
• fragile skin upon mechanical load
• however, the water barrier remains intact




Genotype
MGI:5509366
cx5
Allelic
Composition
Krt1tm1Tmm/Krt1tm1Tmm
S100a9tm1Nck/S100a9tm1Nck
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Krt1tm1Tmm mutation (0 available); any Krt1 mutation (68 available)
S100a9tm1Nck mutation (0 available); any S100a9 mutation (18 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• no survivors are generated




Genotype
MGI:5509364
cx6
Allelic
Composition
Il18tm1Khe/Il18tm1Khe
Krt1tm1Tmm/Krt1tm1Tmm
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Il18tm1Khe mutation (0 available); any Il18 mutation (32 available)
Krt1tm1Tmm mutation (0 available); any Krt1 mutation (68 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
N
• lethality observed in Krt1tm1Tmm heterozygotes is partially rescued

integument
N
• normal epidermal morphology with normal numbers of intact cornified envelops





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