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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Myf6tm1(cre)Mrc
targeted mutation 1, Mario R Capecchi
MGI:3487371
Summary 9 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Myf6tm1(cre)Mrc/Myf6tm1(cre)Mrc involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:3510829
cn2
Myf6tm1(cre)Mrc/Myf6+
Pax3tm1Mrc/Pax3tm1Mrc
Trp53tm1Brn/Trp53+
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL MGI:3844657
cn3
Myf6tm1(cre)Mrc/Myf6+
Pax3tm1Mrc/Pax3tm1Mrc
Trp53tm1Brn/Trp53tm1Brn
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL MGI:3844658
cn4
Gt(ROSA)26Sortm1(DTA)Mrc/Gt(ROSA)26Sor+
Myf6tm1(cre)Mrc/Myf6+
involves: 129S1/Sv * 129X1/SvJ MGI:3783879
cn5
Gt(ROSA)26Sortm3(SS18/EGFP)Mrc/Gt(ROSA)26Sortm3(SS18/EGFP)Mrc
Myf6tm1(cre)Mrc/Myf6tm1(cre)Mrc
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:3710997
cn6
Gt(ROSA)26Sortm2(SS18)Mrc/Gt(ROSA)26Sortm2(SS18)Mrc
Myf6tm1(cre)Mrc/Myf6tm1(cre)Mrc
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:3710996
cn7
Cdkn2atm4Rdp/Cdkn2atm4Rdp
Myf6tm1(cre)Mrc/Myf6+
Pax3tm1Mrc/Pax3tm1Mrc
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL MGI:3844659
cn8
Myf6tm1(cre)Mrc/Myf6+
Pax3tm1Mrc/Pax3+
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL MGI:3844656
cn9
Foxo1tm1Mrc/Foxo1tm1Mrc
Myf6tm1(cre)Mrc/Myf6+
Pax3tm1Mrc/Pax3tm1Mrc
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL MGI:3844661


Genotype
MGI:3510829
hm1
Allelic
Composition
Myf6tm1(cre)Mrc/Myf6tm1(cre)Mrc
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Myf6tm1(cre)Mrc mutation (0 available); any Myf6 mutation (19 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype
• homozygotes are normal and fertile with no rib fusions detected




Genotype
MGI:3844657
cn2
Allelic
Composition
Myf6tm1(cre)Mrc/Myf6+
Pax3tm1Mrc/Pax3tm1Mrc
Trp53tm1Brn/Trp53+
Genetic
Background
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Myf6tm1(cre)Mrc mutation (0 available); any Myf6 mutation (19 available)
Pax3tm1Mrc mutation (1 available); any Pax3 mutation (50 available)
Trp53tm1Brn mutation (18 available); any Trp53 mutation (240 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• 1 in 12 mice develop an rhabdomyosarcoma by day 202

muscle
• 1 in 12 mice develop an rhabdomyosarcoma by day 202

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
alveolar rhabdomyosarcoma DOID:4051 OMIM:268220
J:93444




Genotype
MGI:3844658
cn3
Allelic
Composition
Myf6tm1(cre)Mrc/Myf6+
Pax3tm1Mrc/Pax3tm1Mrc
Trp53tm1Brn/Trp53tm1Brn
Genetic
Background
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Myf6tm1(cre)Mrc mutation (0 available); any Myf6 mutation (19 available)
Pax3tm1Mrc mutation (1 available); any Pax3 mutation (50 available)
Trp53tm1Brn mutation (18 available); any Trp53 mutation (240 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• 2 in 5 mice develop an rhabdomyosarcoma by day 75 to 91

muscle
• 2 in 5 mice develop an rhabdomyosarcoma by day 75 to 91

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
alveolar rhabdomyosarcoma DOID:4051 OMIM:268220
J:93444




Genotype
MGI:3783879
cn4
Allelic
Composition
Gt(ROSA)26Sortm1(DTA)Mrc/Gt(ROSA)26Sor+
Myf6tm1(cre)Mrc/Myf6+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gt(ROSA)26Sortm1(DTA)Mrc mutation (1 available); any Gt(ROSA)26Sor mutation (993 available)
Myf6tm1(cre)Mrc mutation (0 available); any Myf6 mutation (19 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• pups are immobile and die shortly after birth

muscle
• myogenesis appears normal at E12.5
• increasing apoptosis until all differentiating myofibers are either dead or dying at E18.5
• newborns lack differentiated myofibers
• basophilic clumps of cellular debris suggest skeletal muscle forms and then degenerates




Genotype
MGI:3710997
cn5
Allelic
Composition
Gt(ROSA)26Sortm3(SS18/EGFP)Mrc/Gt(ROSA)26Sortm3(SS18/EGFP)Mrc
Myf6tm1(cre)Mrc/Myf6tm1(cre)Mrc
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gt(ROSA)26Sortm3(SS18/EGFP)Mrc mutation (0 available); any Gt(ROSA)26Sor mutation (993 available)
Myf6tm1(cre)Mrc mutation (0 available); any Myf6 mutation (19 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice die by 6 months of age

neoplasm
N
• unlike in other Gt(ROSA)26Sortm3(SS18)Mrc homozygously activated mice, no tumors form

muscle
• myopathy is characterized by abnormal wavy fiber and limited rhabdomyolysis




Genotype
MGI:3710996
cn6
Allelic
Composition
Gt(ROSA)26Sortm2(SS18)Mrc/Gt(ROSA)26Sortm2(SS18)Mrc
Myf6tm1(cre)Mrc/Myf6tm1(cre)Mrc
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gt(ROSA)26Sortm2(SS18)Mrc mutation (0 available); any Gt(ROSA)26Sor mutation (993 available)
Myf6tm1(cre)Mrc mutation (0 available); any Myf6 mutation (19 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice die by 6 months of age

neoplasm
N
• unlike in other Gt(ROSA)26Sortm2(SS18)Mrc homozygously activated mice, no tumors form

muscle
• intrafiber vacuolation is present in some muscle fibers
• apoptosis of differentiated skeletal muscle fibers is increased
• central nuclei are present in some muscle fibers
• myopathy is characterized by abnormal wavy fiber and limited rhabdomyolysis




Genotype
MGI:3844659
cn7
Allelic
Composition
Cdkn2atm4Rdp/Cdkn2atm4Rdp
Myf6tm1(cre)Mrc/Myf6+
Pax3tm1Mrc/Pax3tm1Mrc
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdkn2atm4Rdp mutation (0 available); any Cdkn2a mutation (67 available)
Myf6tm1(cre)Mrc mutation (0 available); any Myf6 mutation (19 available)
Pax3tm1Mrc mutation (1 available); any Pax3 mutation (50 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• 4 in 14 mice develop an rhabdomyosarcoma by day 56 to 89

muscle
• 4 in 14 mice develop an rhabdomyosarcoma by day 56 to 89

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
alveolar rhabdomyosarcoma DOID:4051 OMIM:268220
J:93444




Genotype
MGI:3844656
cn8
Allelic
Composition
Myf6tm1(cre)Mrc/Myf6+
Pax3tm1Mrc/Pax3+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Myf6tm1(cre)Mrc mutation (0 available); any Myf6 mutation (19 available)
Pax3tm1Mrc mutation (1 available); any Pax3 mutation (50 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• 1 in 228 mice develop an rhabdomyosarcoma that arises from the pectoralis major muscle by day 383

muscle
• 1 in 228 mice develop an rhabdomyosarcoma that arises from the pectoralis major muscle by day 383

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
alveolar rhabdomyosarcoma DOID:4051 OMIM:268220
J:93444




Genotype
MGI:3844661
cn9
Allelic
Composition
Foxo1tm1Mrc/Foxo1tm1Mrc
Myf6tm1(cre)Mrc/Myf6+
Pax3tm1Mrc/Pax3tm1Mrc
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Foxo1tm1Mrc mutation (0 available); any Foxo1 mutation (32 available)
Myf6tm1(cre)Mrc mutation (0 available); any Myf6 mutation (19 available)
Pax3tm1Mrc mutation (1 available); any Pax3 mutation (50 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
N
• mice do not exhibit accelerated tumorigenesis





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