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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Otulintm1c(EUCOMM)Hmgu
targeted mutation 1c, Helmholtz Zentrum Muenchen GmbH
MGI:6449230
Summary 7 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Myd88tm1Aki/Myd88tm1Aki
Otulintm1c(EUCOMM)Hmgu/Otulintm1c(EUCOMM)Hmgu
Tg(KRT14-cre)1Cgn/0
involves: 129P2/OlaHsd * C57BL/6 * C57BL/6N * DBA/2 MGI:7256624
cn2
Ifnar1tm1Agt/Ifnar1tm1Agt
Otulintm1c(EUCOMM)Hmgu/Otulintm1c(EUCOMM)Hmgu
Tg(KRT14-cre)1Cgn/0
involves: 129S2/SvPas * C57BL/6 * C57BL/6N * DBA/2 MGI:7256625
cn3
Otulintm1c(EUCOMM)Hmgu/Otulintm1c(EUCOMM)Hmgu
Tg(KRT14-cre)1Cgn/0
Tnfrsf1atm1Mak/Tnfrsf1atm1Mak
involves: 129S2/SvPas * C57BL/6 * C57BL/6N * DBA/2 MGI:7256612
cn4
Otulinem1Gvl/Otulintm1c(EUCOMM)Hmgu
Tg(KRT14-cre)1Cgn/0
involves: C57BL/6 * C57BL/6J * C57BL/6N * DBA/2 MGI:7256600
cn5
Mlkltm1.1Wsa/Mlkltm1.1Wsa
Otulintm1c(EUCOMM)Hmgu/Otulintm1c(EUCOMM)Hmgu
Tg(KRT14-cre)1Cgn/0
involves: C57BL/6 * C57BL/6N * DBA/2 MGI:7256622
cn6
Faddtm1Mpa/Faddtm1Mpa
Mlkltm1.1Wsa/Mlkltm1.1Wsa
Otulintm1c(EUCOMM)Hmgu/Otulintm1c(EUCOMM)Hmgu
Tg(KRT14-cre)1Cgn/0
involves: C57BL/6 * C57BL/6N * DBA/2 MGI:7256619
cn7
Otulintm1c(EUCOMM)Hmgu/Otulintm1c(EUCOMM)Hmgu
Tg(KRT14-cre)1Cgn/0
involves: C57BL/6 * C57BL/6N * DBA/2 MGI:7256626


Genotype
MGI:7256624
cn1
Allelic
Composition
Myd88tm1Aki/Myd88tm1Aki
Otulintm1c(EUCOMM)Hmgu/Otulintm1c(EUCOMM)Hmgu
Tg(KRT14-cre)1Cgn/0
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6 * C57BL/6N * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Myd88tm1Aki mutation (9 available); any Myd88 mutation (52 available)
Otulintm1c(EUCOMM)Hmgu mutation (0 available); any Otulin mutation (24 available)
Tg(KRT14-cre)1Cgn mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
integument
N
• no skin lesions and normal epidermal thickness




Genotype
MGI:7256625
cn2
Allelic
Composition
Ifnar1tm1Agt/Ifnar1tm1Agt
Otulintm1c(EUCOMM)Hmgu/Otulintm1c(EUCOMM)Hmgu
Tg(KRT14-cre)1Cgn/0
Genetic
Background
involves: 129S2/SvPas * C57BL/6 * C57BL/6N * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ifnar1tm1Agt mutation (11 available); any Ifnar1 mutation (60 available)
Otulintm1c(EUCOMM)Hmgu mutation (0 available); any Otulin mutation (24 available)
Tg(KRT14-cre)1Cgn mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
N
• normal circulating inflammatory cytokine and chemokine levels in most mice
• delineated inflamed skin lesions from age 6 weeks in some mice

integument
N
• no skin lesions and normal epidermal thickness in most mice
• delineated inflamed skin lesions from age 6 weeks in some mice




Genotype
MGI:7256612
cn3
Allelic
Composition
Otulintm1c(EUCOMM)Hmgu/Otulintm1c(EUCOMM)Hmgu
Tg(KRT14-cre)1Cgn/0
Tnfrsf1atm1Mak/Tnfrsf1atm1Mak
Genetic
Background
involves: 129S2/SvPas * C57BL/6 * C57BL/6N * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Otulintm1c(EUCOMM)Hmgu mutation (0 available); any Otulin mutation (24 available)
Tg(KRT14-cre)1Cgn mutation (2 available)
Tnfrsf1atm1Mak mutation (2 available); any Tnfrsf1a mutation (52 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
N
• normal circulating inflammatory cytokine and chemokine levels

integument
N
• no dermatitis and normal epidermal thickness up to age older than 40 weeks




Genotype
MGI:7256600
cn4
Allelic
Composition
Otulinem1Gvl/Otulintm1c(EUCOMM)Hmgu
Tg(KRT14-cre)1Cgn/0
Genetic
Background
involves: C57BL/6 * C57BL/6J * C57BL/6N * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Otulinem1Gvl mutation (0 available); any Otulin mutation (24 available)
Otulintm1c(EUCOMM)Hmgu mutation (0 available); any Otulin mutation (24 available)
Tg(KRT14-cre)1Cgn mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• delineated inflamed skin lesions on back

integument
• delineated inflamed skin lesions on back
• delineated inflamed skin lesions on back

neoplasm
• verrucous carcinomas on back skin




Genotype
MGI:7256622
cn5
Allelic
Composition
Mlkltm1.1Wsa/Mlkltm1.1Wsa
Otulintm1c(EUCOMM)Hmgu/Otulintm1c(EUCOMM)Hmgu
Tg(KRT14-cre)1Cgn/0
Genetic
Background
involves: C57BL/6 * C57BL/6N * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mlkltm1.1Wsa mutation (0 available); any Mlkl mutation (32 available)
Otulintm1c(EUCOMM)Hmgu mutation (0 available); any Otulin mutation (24 available)
Tg(KRT14-cre)1Cgn mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• delineated inflamed skin lesions on back
• no skin lesions in tail

integument
N
• no skin lesions and normal epidermal thickness in tail
• delineated inflamed skin lesions on back
• no skin lesions in tail




Genotype
MGI:7256619
cn6
Allelic
Composition
Faddtm1Mpa/Faddtm1Mpa
Mlkltm1.1Wsa/Mlkltm1.1Wsa
Otulintm1c(EUCOMM)Hmgu/Otulintm1c(EUCOMM)Hmgu
Tg(KRT14-cre)1Cgn/0
Genetic
Background
involves: C57BL/6 * C57BL/6N * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Faddtm1Mpa mutation (0 available); any Fadd mutation (18 available)
Mlkltm1.1Wsa mutation (0 available); any Mlkl mutation (32 available)
Otulintm1c(EUCOMM)Hmgu mutation (0 available); any Otulin mutation (24 available)
Tg(KRT14-cre)1Cgn mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
N
• normal circulating inflammatory cytokine levels

integument
N
• no skin lesions and normal epidermal thickness




Genotype
MGI:7256626
cn7
Allelic
Composition
Otulintm1c(EUCOMM)Hmgu/Otulintm1c(EUCOMM)Hmgu
Tg(KRT14-cre)1Cgn/0
Genetic
Background
involves: C57BL/6 * C57BL/6N * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Otulintm1c(EUCOMM)Hmgu mutation (0 available); any Otulin mutation (24 available)
Tg(KRT14-cre)1Cgn mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
integument
• increased hair follicle stem cell (HFSC) and interfollicular epidermis (IFE) cell apoptosis
• in both skin lesions and non-lesional skin at age 7 weeks
• hyperproliferation
• accelerated wound closure at day 2 and 4 post-wounding
• decelerated wound closure at day 8 post-wounding
• hypersebacea at age 7 weeks
• at wound sites after completion of re-epithelialization
• of back and tail skin lesions at age 7 weeks
• normal in non-lesional skin
• delineated inflamed skin lesions on back and tail from age P6 onwards
• infiltration of immune cells into lesional skin
• of back and tail skin lesions at age 7 weeks
• normal epidermal thickness of non-lesional skin
• tumor-like lesions at wound sites after completion of re-epithelialization
• delineated inflamed skin lesions on back and tail from age P6 onwards
• verrucous carcinoma developed from back and tail skin lesions

neoplasm
• verrucous carcinoma developed from back and tail skin lesions

immune system
• delineated inflamed skin lesions on back and tail from age P6 onwards
• infiltration of immune cells into lesional skin

cellular
• increased hair follicle stem cell (HFSC) and interfollicular epidermis (IFE) cell apoptosis
• in both skin lesions and non-lesional skin at age 7 weeks
• hyperproliferation
• accelerated wound closure at day 2 and 4 post-wounding
• decelerated wound closure at day 8 post-wounding

endocrine/exocrine glands
• hypersebacea at age 7 weeks

homeostasis/metabolism
• of back and tail skin lesions at age 7 weeks
• normal in non-lesional skin

growth/size/body
• at wound sites after completion of re-epithelialization

embryo
N
• born at normal Mendelian ratios





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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory