About   Help   FAQ
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)





Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
05/07/2024
MGI 6.23
The Jackson Laboratory