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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Braftm1Sva
targeted mutation 1, Alcino J Silva
MGI:3620008
Summary 12 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Braftm1Sva/Braftm1Sva
Krastm1Bbd/Kras+
Polr2atm1(cre/ERT2)Bbd/Polr2atm1(cre/ERT2)Bbd
Raf1tm2Bacc/Raf1tm2Bacc
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ MGI:5508357
cn2
Braftm1Sva/Braftm1Sva
Polr2atm1(cre/ERT2)Bbd/Polr2atm1(cre/ERT2)Bbd
Raf1tm2Bacc/Raf1tm2Bacc
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ MGI:5508350
cn3
Braftm1Sva/Braftm1Sva
Raf1tm2Bacc/Raf1tm2Bacc
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:3713578
cn4
Braftm1Sva/Braftm1.1Sva
Raf1tm1Bacc/Raf1tm2Bacc
Tg(Nes-cre)1Kln/0
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL MGI:3713581
cn5
Braftm1Sva/Braftm1Sva
Raf1tm2Bacc/Raf1+
Tg(Nes-cre)1Kln/0
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL MGI:3713555
cn6
Braftm1Sva/Braf+
Raf1tm2Bacc/Raf1tm2Bacc
Tg(Nes-cre)1Kln/0
involves: 129P2/OlaHsd * C57BL/6 * SJL MGI:3713653
cn7
Braftm1Sva/Braftm1.1Sva
Meox2tm1(cre)Sor/Meox2+
involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ MGI:3622484
cn8
Braftm1Sva/Braftm1Sva
Tg(Tek-cre/ERT2)1Arnd/0
involves: 129S1/Sv * 129T2/SvEms * 129X1/SvJ MGI:3622482
cn9
Braftm1Sva/Braftm1Sva
Tg(Camk2a-cre)1557Sva/0
involves: 129S1/Sv * 129T2/SvEms * 129X1/SvJ * FVB MGI:3622479
cn10
Braftm1Sva/Braftm1Sva
Krastm1Bbd/Kras+
involves: 129S1/Sv * 129X1/SvJ MGI:5508329
cn11
Braftm1Sva/Braftm1Sva
Krastm1Bbd/Kras+
Polr2atm1(cre/ERT2)Bbd/Polr2atm1(cre/ERT2)Bbd
involves: 129S1/Sv * 129X1/SvJ MGI:5508351
cn12
Braftm1Sva/Braftm1.1Sva
Tg(Nes-cre)1Kln/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL MGI:3713552


Genotype
MGI:5508357
cn1
Allelic
Composition
Braftm1Sva/Braftm1Sva
Krastm1Bbd/Kras+
Polr2atm1(cre/ERT2)Bbd/Polr2atm1(cre/ERT2)Bbd
Raf1tm2Bacc/Raf1tm2Bacc
Genetic
Background
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Braftm1Sva mutation (1 available); any Braf mutation (58 available)
Krastm1Bbd mutation (2 available); any Kras mutation (76 available)
Polr2atm1(cre/ERT2)Bbd mutation (3 available); any Polr2a mutation (92 available)
Raf1tm2Bacc mutation (0 available); any Raf1 mutation (114 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• primary mouse embryonic fibroblasts exposed to 4OHT for 5 days to activate cre/ERT2 recombinase exhibit decreased proliferation that is similar to that in single Kras mutants without further additive effects




Genotype
MGI:5508350
cn2
Allelic
Composition
Braftm1Sva/Braftm1Sva
Polr2atm1(cre/ERT2)Bbd/Polr2atm1(cre/ERT2)Bbd
Raf1tm2Bacc/Raf1tm2Bacc
Genetic
Background
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Braftm1Sva mutation (1 available); any Braf mutation (58 available)
Polr2atm1(cre/ERT2)Bbd mutation (3 available); any Polr2a mutation (92 available)
Raf1tm2Bacc mutation (0 available); any Raf1 mutation (114 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype
• 30 day old mice fed a tamoxifen diet for 3 months are healthy and show normal weight and activity and no obvious anatomical defects




Genotype
MGI:3713578
cn3
Allelic
Composition
Braftm1Sva/Braftm1Sva
Raf1tm2Bacc/Raf1tm2Bacc
Genetic
Background
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Braftm1Sva mutation (1 available); any Braf mutation (58 available)
Raf1tm2Bacc mutation (0 available); any Raf1 mutation (114 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• cultured DRG neurons transfected with Cre-EGFP have very short axons, compared to long and dense axon networks formed by control neurons

cellular
• cultured DRG neurons transfected with Cre-EGFP have very short axons, compared to long and dense axon networks formed by control neurons




Genotype
MGI:3713581
cn4
Allelic
Composition
Braftm1Sva/Braftm1.1Sva
Raf1tm1Bacc/Raf1tm2Bacc
Tg(Nes-cre)1Kln/0
Genetic
Background
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Braftm1.1Sva mutation (0 available); any Braf mutation (58 available)
Braftm1Sva mutation (1 available); any Braf mutation (58 available)
Raf1tm1Bacc mutation (0 available); any Raf1 mutation (114 available)
Raf1tm2Bacc mutation (0 available); any Raf1 mutation (114 available)
Tg(Nes-cre)1Kln mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• no double conditional embryos are found live at E14-15, but can be isolated at E13

nervous system
• DRG neurons cultured with NGF for 5 days show impaired axon outgrowth
• sensory nerve trunks form normally, but distal arborization is reduced compared to controls
• at E13, Ret levels in DRGs are reduced

cellular
• DRG neurons cultured with NGF for 5 days show impaired axon outgrowth




Genotype
MGI:3713555
cn5
Allelic
Composition
Braftm1Sva/Braftm1Sva
Raf1tm2Bacc/Raf1+
Tg(Nes-cre)1Kln/0
Genetic
Background
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Braftm1Sva mutation (1 available); any Braf mutation (58 available)
Raf1tm2Bacc mutation (0 available); any Raf1 mutation (114 available)
Tg(Nes-cre)1Kln mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• most die before weaning

growth/size/body
• mice are smaller in the postnatal period than Braf conditional knockouts

nervous system
• deficiency of terminal axonal projections of parvalbumin-positive neurons toward the lateral motor pools of the spinal cord is seen compared to controls
• proprioceptive axons enter spinal cord normally, but few progress beyond intermediate zone
• at P12, number of Ret+ neurons in DRG is reduced; numbers of CGRG+ neurons are increased




Genotype
MGI:3713653
cn6
Allelic
Composition
Braftm1Sva/Braf+
Raf1tm2Bacc/Raf1tm2Bacc
Tg(Nes-cre)1Kln/0
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Braftm1Sva mutation (1 available); any Braf mutation (58 available)
Raf1tm2Bacc mutation (0 available); any Raf1 mutation (114 available)
Tg(Nes-cre)1Kln mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype
• mice show no phenotypic abnormalities at any stage




Genotype
MGI:3622484
cn7
Allelic
Composition
Braftm1Sva/Braftm1.1Sva
Meox2tm1(cre)Sor/Meox2+
Genetic
Background
involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Braftm1.1Sva mutation (0 available); any Braf mutation (58 available)
Braftm1Sva mutation (1 available); any Braf mutation (58 available)
Meox2tm1(cre)Sor mutation (3 available); any Meox2 mutation (18 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• although born alive death occurs around 21 days of age from aggressive neurodegenerative disease

growth/size/body
• after being born alive, pups show progressive growth retardation




Genotype
MGI:3622482
cn8
Allelic
Composition
Braftm1Sva/Braftm1Sva
Tg(Tek-cre/ERT2)1Arnd/0
Genetic
Background
involves: 129S1/Sv * 129T2/SvEms * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Braftm1Sva mutation (1 available); any Braf mutation (58 available)
Tg(Tek-cre/ERT2)1Arnd mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype




Genotype
MGI:3622479
cn9
Allelic
Composition
Braftm1Sva/Braftm1Sva
Tg(Camk2a-cre)1557Sva/0
Genetic
Background
involves: 129S1/Sv * 129T2/SvEms * 129X1/SvJ * FVB
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Braftm1Sva mutation (1 available); any Braf mutation (58 available)
Tg(Camk2a-cre)1557Sva mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• six month old mice have poor context discrimination although contextual conditioning is normal
• six month old mice much slower to learn the platform position in a hidden platform Morris water maze (Motor coordination normal)

nervous system
• six month old mice are deficient in the early phase of long term potentiation although there is no disruption of synaptic transmission or presynaptic plasticity




Genotype
MGI:5508329
cn10
Allelic
Composition
Braftm1Sva/Braftm1Sva
Krastm1Bbd/Kras+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Braftm1Sva mutation (1 available); any Braf mutation (58 available)
Krastm1Bbd mutation (2 available); any Kras mutation (76 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• following intratracheal instillation of adenovirus expressing Cre-recombinase (Ad-Cre), mice show 50% survival at 41.5 weeks compared to 40 weeks in single Kras heterozygous controls, indicating similar survival

neoplasm
• mice develop non-small cell lung carcinoma following intratracheal instillation of adenovirus expressing Cre-recombinase (Ad-Cre); tumor burden in similar to that seen in single Kras heterozygotes

respiratory system
• mice develop non-small cell lung carcinoma following intratracheal instillation of adenovirus expressing Cre-recombinase (Ad-Cre); tumor burden in similar to that seen in single Kras heterozygotes




Genotype
MGI:5508351
cn11
Allelic
Composition
Braftm1Sva/Braftm1Sva
Krastm1Bbd/Kras+
Polr2atm1(cre/ERT2)Bbd/Polr2atm1(cre/ERT2)Bbd
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Braftm1Sva mutation (1 available); any Braf mutation (58 available)
Krastm1Bbd mutation (2 available); any Kras mutation (76 available)
Polr2atm1(cre/ERT2)Bbd mutation (3 available); any Polr2a mutation (92 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• primary mouse embryonic fibroblasts exposed to 4OHT for 5 days to activate cre/ERT2 recombinase exhibit decreased proliferation compared to single Kras heterozygotes




Genotype
MGI:3713552
cn12
Allelic
Composition
Braftm1Sva/Braftm1.1Sva
Tg(Nes-cre)1Kln/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Braftm1.1Sva mutation (0 available); any Braf mutation (58 available)
Braftm1Sva mutation (1 available); any Braf mutation (58 available)
Tg(Nes-cre)1Kln mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice tend to die in third week postnatal, although some survive to P35

growth/size/body
• at P32, body weight is ~25% of littermates
• from P12-14 onwards, mice show severe growth retardation

behavior/neurological
N
• mice show normal nociceptive response in hotplate assay
• mice appear hyperactive

nervous system
N
• dorsal root ganglion neurons survive in mutants
• perivascular hypothalamic axonal innervation is reduced
• anterior lobe of pituitary gland is markedly reduced in size compared to controls
• disproportionate thinning of cortex is observed

endocrine/exocrine glands
• perivascular hypothalamic axonal innervation is reduced
• anterior lobe of pituitary gland is markedly reduced in size compared to controls

homeostasis/metabolism
• mice display significantly reduced bolood glucose levels
• when separated from other mice, body temperature drops rapidly
• level is elevated in pituitary relative to controls
• level of growth hormone is elevated in individual pituitary endocrine cells





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last database update
05/07/2024
MGI 6.23
The Jackson Laboratory