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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(KRT14-Kitl)1Takk
transgene insertion 1, Takahiro Kunisada
MGI:3607790
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cx1
Mc1re/Mc1re
Xpctm1Brd/Xpctm1Brd
Tg(KRT14-Kitl)1Takk/0
involves: 129S7/SvEvBrd * C57BL/6 * SJL MGI:3686788
cx2
Xpatm1Tnka/Xpatm1Tnka
Tg(KRT14-Kitl)1Takk/?
involves: C57BL/6 * CBA * SJL MGI:4361120
cx3
Mc1re/Mc1re
Tg(KRT14-Kitl)1Takk/0
involves: C57BL/6 * SJL MGI:3686789


Genotype
MGI:3686788
cx1
Allelic
Composition
Mc1re/Mc1re
Xpctm1Brd/Xpctm1Brd
Tg(KRT14-Kitl)1Takk/0
Genetic
Background
involves: 129S7/SvEvBrd * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mc1re mutation (4 available); any Mc1r mutation (44 available)
Tg(KRT14-Kitl)1Takk mutation (1 available)
Xpctm1Brd mutation (1 available); any Xpc mutation (34 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• vehicle-treated mutants show weight loss, indicative of failure to thrive, compared to forskolin-treated animals

neoplasm
• vehicle-treated mutant controls develop tumors more rapidly (11 tumors ~4 weeks after 20 weeks of UV-B exposure) compared to forskolin-treated mice (6 tumors, onset ~25 weeks)
• other types of tumors are found in vehicle-treated mice (3/11); 2/9 mice develop multiple tumors
• tumors in vehicle-treated mutants are mainly this type (6/11) while forskolin-treated mice develop only this type

integument
• vehicle-treated mutants show significant sun damage after 20 weeks of UV-B exposure including profound epidermal thickening while forskoling treatment prevented damage
• vehicle-treated mutants show evidence of sun damage like scarring after 20 weeks of UV-B exposure while forskolin treatment prevented damage




Genotype
MGI:4361120
cx2
Allelic
Composition
Xpatm1Tnka/Xpatm1Tnka
Tg(KRT14-Kitl)1Takk/?
Genetic
Background
involves: C57BL/6 * CBA * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(KRT14-Kitl)1Takk mutation (1 available)
Xpatm1Tnka mutation (0 available); any Xpa mutation (21 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
pigmentation

neoplasm
• mice irradiated with UV-B 3X/week for 10 weeks, total dose 150J/cm2
• unevenly pigmented macules appear on re-epithelialized skin at 4 months after UV-B exposure
• lentigo maligna melanomas eventually become elevated tumors
• black nodular melanomas in some mice by 6 months after exposure
• at 53 weeks, 8 of 61 mice with nodular melanomas and 12 of 61 mice show lintigo maligna melanoma
• one type of tumor or the other, never both
• melanoma cells invade the dermis
• both types of melanomas become metastatic

integument
• mice irradiated with UV-B 3X/week for 10 weeks, total dose 150J/cm2
• unevenly pigmented macules appear on re-epithelialized skin at 4 months after UV-B exposure
• lentigo maligna melanomas eventually become elevated tumors
• black nodular melanomas in some mice by 6 months after exposure
• at 53 weeks, 8 of 61 mice with nodular melanomas and 12 of 61 mice show lintigo maligna melanoma
• one type of tumor or the other, never both

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
skin melanoma DOID:8923 OMIM:608035
OMIM:612263
J:100608




Genotype
MGI:3686789
cx3
Allelic
Composition
Mc1re/Mc1re
Tg(KRT14-Kitl)1Takk/0
Genetic
Background
involves: C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mc1re mutation (4 available); any Mc1r mutation (44 available)
Tg(KRT14-Kitl)1Takk mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
pigmentation
• in mutants, no measurable UV-induced melanization is observed; forskolin application to the skin induces significant skin darkening





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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
10/29/2024
MGI 6.24
The Jackson Laboratory