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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(NES-TVA)J12Ech
transgene insertion J12, Eric C Holland
MGI:2663944
Summary 8 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cx1
Tg(NES-TVA)J12Ech/0
Trp53tm1Brd/Trp53+
involves: 129 * C57BL/6 * FVB/N MGI:3835348
cx2
Cdkn2atm1Rdp/Cdkn2a+
Tg(NES-TVA)J12Ech/0
involves: 129 * C57BL/6 * FVB/N * SJL MGI:3835347
cx3
Cdkn2atm1Rdp/Cdkn2atm1Rdp
Tg(NES-TVA)J12Ech/0
involves: 129 * C57BL/6 * FVB/N * SJL MGI:3835346
cx4
Cdkn2atm2.1Rdp/Cdkn2atm2.1Rdp
Tg(NES-TVA)J12Ech/0
involves: 129S6/SvEvTac * C57BL/6 * FVB/N MGI:3835366
cx5
Cdkn2atm1Rdp/Cdkn2atm1Rdp
Tg(NES-TVA)J12Ech/0
involves: 129/Sv * C57BL/6 * FVB/N * SJL MGI:3835361
cx6
Cdkn2atm1Cjs/Cdkn2atm1Cjs
Tg(NES-TVA)J12Ech/0
involves: 129X1/SvJ * C57BL/6 * FVB/N MGI:3835358
tg7
Tg(NES-TVA)J12Ech/0 involves: 129 * C57BL/6 * FVB/N MGI:3835345
tg8
Tg(NES-TVA)J12Ech/0 involves: FVB/N MGI:3835357


Genotype
MGI:3835348
cx1
Allelic
Composition
Tg(NES-TVA)J12Ech/0
Trp53tm1Brd/Trp53+
Genetic
Background
involves: 129 * C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(NES-TVA)J12Ech mutation (2 available)
Trp53tm1Brd mutation (5 available); any Trp53 mutation (232 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• 3 of 8 mice transfected with replication-competent ALV splice acceptor viral vector expressing a constitutively active EGFR and Cdk4 develop gliomas compared to 1 of 8 similarly treated wild-type mice
• 17 of 39 mice transfected with replication-competent ALV splice acceptor viral vector expressing a constitutively active EGFR, Cdk4, and bFGF develop gliomas compared to 3 of 29 similarly treated wild-type mice
• however, mice transfected with replication-competent ALV splice acceptor viral vector expressing a constitutively active EGFR do not develop gliomas
• in mice transfected with replication-competent ALV splice acceptor viral vector expressing a constitutively active EGFR, Cdk4, and bFGF

neoplasm
• 3 of 8 mice transfected with replication-competent ALV splice acceptor viral vector expressing a constitutively active EGFR and Cdk4 develop gliomas compared to 1 of 8 similarly treated wild-type mice
• 17 of 39 mice transfected with replication-competent ALV splice acceptor viral vector expressing a constitutively active EGFR, Cdk4, and bFGF develop gliomas compared to 3 of 29 similarly treated wild-type mice
• however, mice transfected with replication-competent ALV splice acceptor viral vector expressing a constitutively active EGFR do not develop gliomas




Genotype
MGI:3835347
cx2
Allelic
Composition
Cdkn2atm1Rdp/Cdkn2a+
Tg(NES-TVA)J12Ech/0
Genetic
Background
involves: 129 * C57BL/6 * FVB/N * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdkn2atm1Rdp mutation (6 available); any Cdkn2a mutation (62 available)
Tg(NES-TVA)J12Ech mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• 13 of 25 mice transfected with replication-competent ALV splice acceptor viral vector expressing a constitutively active EGFR develop gliomas unlike similarly treated wild-type mice

nervous system
• 13 of 25 mice transfected with replication-competent ALV splice acceptor viral vector expressing a constitutively active EGFR develop gliomas unlike similarly treated wild-type mice




Genotype
MGI:3835346
cx3
Allelic
Composition
Cdkn2atm1Rdp/Cdkn2atm1Rdp
Tg(NES-TVA)J12Ech/0
Genetic
Background
involves: 129 * C57BL/6 * FVB/N * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdkn2atm1Rdp mutation (6 available); any Cdkn2a mutation (62 available)
Tg(NES-TVA)J12Ech mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• 8 of 19 mice transfected with replication-competent ALV splice acceptor viral vector expressing a constitutively active EGFR develop gliomas unlike similarly treated wild-type mice
• 4 of 10 mice transfected with replication-competent ALV splice acceptor viral vector expressing a constitutively active EGFR and Cdk4 develop gliomas compared to 1 of 8 similarly treated wild-type mice
• 6 of 16 mice transfected with replication-competent ALV splice acceptor viral vector expressing a constitutively active EGFR, Cdk4, and bFGF develop gliomas compared to 3 of 29 similarly treated wild-type mice
• in mice transfected with replication-competent ALV splice acceptor viral vector expressing a constitutively active EGFR and bFGF or Cdk4

neoplasm
• 8 of 19 mice transfected with replication-competent ALV splice acceptor viral vector expressing a constitutively active EGFR develop gliomas unlike similarly treated wild-type mice
• 4 of 10 mice transfected with replication-competent ALV splice acceptor viral vector expressing a constitutively active EGFR and Cdk4 develop gliomas compared to 1 of 8 similarly treated wild-type mice
• 6 of 16 mice transfected with replication-competent ALV splice acceptor viral vector expressing a constitutively active EGFR, Cdk4, and bFGF develop gliomas compared to 3 of 29 similarly treated wild-type mice




Genotype
MGI:3835366
cx4
Allelic
Composition
Cdkn2atm2.1Rdp/Cdkn2atm2.1Rdp
Tg(NES-TVA)J12Ech/0
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdkn2atm2.1Rdp mutation (2 available); any Cdkn2a mutation (62 available)
Tg(NES-TVA)J12Ech mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• after 84 days, mice transfected with replication-competent ALV splice acceptor viral vector expressing PDGFB exhibit 20% compared to 50% survival in similarly treated Tg(NES-TVA)12Hev mice

neoplasm
• 22 gliomas are discovered in 28 mice transfected with replication-competent ALV splice acceptor viral vector expressing PDGFB
• 21 grade II (similar to human oligodendroglioma) and 1 grade III (similar to anaplastic oligodendroglioma)

nervous system
• 22 gliomas are discovered in 28 mice transfected with replication-competent ALV splice acceptor viral vector expressing PDGFB
• 21 grade II (similar to human oligodendroglioma) and 1 grade III (similar to anaplastic oligodendroglioma)




Genotype
MGI:3835361
cx5
Allelic
Composition
Cdkn2atm1Rdp/Cdkn2atm1Rdp
Tg(NES-TVA)J12Ech/0
Genetic
Background
involves: 129/Sv * C57BL/6 * FVB/N * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdkn2atm1Rdp mutation (6 available); any Cdkn2a mutation (62 available)
Tg(NES-TVA)J12Ech mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• after 84 days, mice transfected with replication-competent ALV splice acceptor viral vector expressing PDGFB exhibit 15% compared to 50% survival in similarly treated Tg(NES-TVA)12Hev mice (J:125535)
• co delivery of RCAS-PDGFB and an antisense construct targeting Igfbp2 results in improved survival compared to mice infected with RCAS-PDGFB alone (J:153220)

neoplasm
• 17 gliomas are discovered in 20 mice transfected with replication-competent ALV splice acceptor viral vector expressing PDGFB
• 6 grade II (similar to human oligodendroglioma) and 11 grade III (similar to anaplastic oligodendroglioma)
• infection with RCAS-PDGFB induces anaplastic oligodendrogliomas in 97% of mice
• tumors are highly aggressive and display multiple foci of pseudopalisading necrosis and microvascular proliferation
• co-infection with RCAS-PDGFB and RCAS-IGFBP2 results in tumors that are histopathologically identical to those in mice infected with only RCAS-PDGFB
• co delivery of RCAS-PDGFB and an antisense construct targeting Igfbp2 results in a primarily anaplastic oligodendrogliomas but 18% of tumors are lower grade oligodendrogliomas

nervous system
• 17 gliomas are discovered in 20 mice transfected with replication-competent ALV splice acceptor viral vector expressing PDGFB
• 6 grade II (similar to human oligodendroglioma) and 11 grade III (similar to anaplastic oligodendroglioma)
• infection with RCAS-PDGFB induces anaplastic oligodendrogliomas in 97% of mice
• tumors are highly aggressive and display multiple foci of pseudopalisading necrosis and microvascular proliferation
• co-infection with RCAS-PDGFB and RCAS-IGFBP2 results in tumors that are histopathologically identical to those in mice infected with only RCAS-PDGFB
• co delivery of RCAS-PDGFB and an antisense construct targeting Igfbp2 results in a primarily anaplastic oligodendrogliomas but 18% of tumors are lower grade oligodendrogliomas

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
oligodendroglioma DOID:3181 J:153220




Genotype
MGI:3835358
cx6
Allelic
Composition
Cdkn2atm1Cjs/Cdkn2atm1Cjs
Tg(NES-TVA)J12Ech/0
Genetic
Background
involves: 129X1/SvJ * C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdkn2atm1Cjs mutation (6 available); any Cdkn2a mutation (62 available)
Tg(NES-TVA)J12Ech mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• after 84 days, mice transfected with replication-competent ALV splice acceptor viral vector expressing PDGFB exhibit 40% compared to 50% survival in similarly treated Tg(NES-TVA)12Hev mice

neoplasm
• 22 gliomas are discovered in 35 mice transfected with replication-competent ALV splice acceptor viral vector expressing PDGFB
• 10 grade II (similar to human oligodendroglioma) and 12 grade III (similar to anaplastic oligodendroglioma)

nervous system
• 22 gliomas are discovered in 35 mice transfected with replication-competent ALV splice acceptor viral vector expressing PDGFB
• 10 grade II (similar to human oligodendroglioma) and 12 grade III (similar to anaplastic oligodendroglioma)




Genotype
MGI:3835345
tg7
Allelic
Composition
Tg(NES-TVA)J12Ech/0
Genetic
Background
involves: 129 * C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(NES-TVA)J12Ech mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
N
• mice transfected with replication-competent ALV splice acceptor viral vector expressing a constitutively active EGFR do not develop gliomas




Genotype
MGI:3835357
tg8
Allelic
Composition
Tg(NES-TVA)J12Ech/0
Genetic
Background
involves: FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(NES-TVA)J12Ech mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• after 84 days, mice transfected with replication-competent ALV splice acceptor viral vector expressing PDGFB exhibit 50% survival

neoplasm
• 14 gliomas are discovered in 28 mice transfected with replication-competent ALV splice acceptor viral vector expressing PDGFB
• 11 grade II (similar to human oligodendroglioma) and 3 grade III (similar to anaplastic oligodendroglioma)

nervous system
• 14 gliomas are discovered in 28 mice transfected with replication-competent ALV splice acceptor viral vector expressing PDGFB
• 11 grade II (similar to human oligodendroglioma) and 3 grade III (similar to anaplastic oligodendroglioma)





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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory