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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(KRT5-Tert)8043Blas
transgene insertion 8043, Maria A Blasco
MGI:2429416
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cx1
Terctm1Rdp/Terctm1Rdp
Tg(KRT5-Tert)8043Blas/0
involves: 129/Sv * C57BL/6 * C57BL/6J * DBA/2 * SJL MGI:3700845
cx2
Tg(KRT5-Terf2)PMBlas/Y
Tg(KRT5-Tert)8043Blas/0
involves: C57BL/6 * CBA * DBA/2 MGI:6258420
tg3
Tg(KRT5-Tert)8043Blas/0 involves: C57BL/6 * DBA/2 MGI:3700914


Genotype
MGI:3700845
cx1
Allelic
Composition
Terctm1Rdp/Terctm1Rdp
Tg(KRT5-Tert)8043Blas/0
Genetic
Background
involves: 129/Sv * C57BL/6 * C57BL/6J * DBA/2 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Terctm1Rdp mutation (4 available); any Terc mutation (8 available)
Tg(KRT5-Tert)8043Blas mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• mutants exhibit an increase in the frequency of chromosome aberrations in keratinocytes, in particular, of end-to-end fusions, breaks, and telomere associations
• keratinocytes exhibit a significant decrease in average telomere length compared with wild-type cells, similar to that seen in mutant Terc homozygotes

homeostasis/metabolism
• mutants are less susceptible to DMBA + TPA induced skin tumorigenesis, with only 40% developing papillomas compared to 80%, 72% and 86% of wild-type, Tg(KRT5-Tert)8043Blas mutants, and Terc homozygous mutants, respectively
• the number of papillomas per mouse at week 15 is reduced compared to the above controls and papillomas never progress to lesions larger than 3 mm
• mutants exhibit a delayed rate of wound healing in skin compared to Tg(KRT5-Tert)8043Blas mutants

neoplasm
• mutants are less susceptible to DMBA + TPA induced skin tumorigenesis, with only 40% developing papillomas compared to 80%, 72% and 86% of wild-type, Tg(KRT5-Tert)8043Blas mutants, and Terc homozygous mutants, respectively
• the number of papillomas per mouse at week 15 is reduced compared to the above controls and papillomas never progress to lesions larger than 3 mm




Genotype
MGI:6258420
cx2
Allelic
Composition
Tg(KRT5-Terf2)PMBlas/Y
Tg(KRT5-Tert)8043Blas/0
Genetic
Background
involves: C57BL/6 * CBA * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
No mouse lines available in IMSR.
See publication links below for author information.
phenotype observed in females
phenotype observed in males
N normal phenotype
pigmentation
• double mutant mice exhibit skin hyperpigmentation in response to light, similar to single Tg(KRT5-Terf2)PMBlas mutant mice

integument
• double mutant mice exhibit skin hyperpigmentation in response to light, similar to single Tg(KRT5-Terf2)PMBlas mutant mice

cellular
• double mutant mice exhibit short telomeres in tail skin, similar to single Tg(KRT5-Terf2)PMBlas mutant mice, indicating that critically short telomeres are not rescued by telomerase overexpression




Genotype
MGI:3700914
tg3
Allelic
Composition
Tg(KRT5-Tert)8043Blas/0
Genetic
Background
involves: C57BL/6 * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
No mouse lines available in IMSR.
See publication links below for author information.
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
• epidermis is more susceptible to the development of skin tumors upon chemical carcinogenesis (DMBA + TPA), with an increase in the number of papillomas and an increase in mortality (J:69757)
• mutant mice are more susceptible to skin tumorigenesis induced by DMBA + TPA, developing about 1.5-fold more papillomas per mouse than wild-type at week 15 and papillomas progress to bigger lesions (J:96945)
• epidermis shows an increase in wound healing rate compared to wild-type (J:69757)

neoplasm
• epidermis is more susceptible to the development of skin tumors upon chemical carcinogenesis (DMBA + TPA), with an increase in the number of papillomas and an increase in mortality (J:69757)
• mutant mice are more susceptible to skin tumorigenesis induced by DMBA + TPA, developing about 1.5-fold more papillomas per mouse than wild-type at week 15 and papillomas progress to bigger lesions (J:96945)

cellular
N
• mutants exhibit normal telomere length

integument
• TPA-treated skin shows a high number of skin keratinocyte layers (skin hyperplasia) that are not seen in controls, indicating a more sustained proliferative response of skin to TPA treatment (J:69757)





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last database update
11/19/2024
MGI 6.24
The Jackson Laboratory