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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Ptpn11tm1.1Wbm
targeted mutation 1.1, Walter Birchmeier
MGI:4365539
Summary 8 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Ptpn11tm1.1Wbm/Ptpn11tm1.1Wbm involves: 129P2/OlaHsd * C57BL/6 * SJL MGI:4365547
cn2
Egr2tm2(cre)Pch/Egr2+
Gt(ROSA)26Sortm7(Pik3ca*,EGFP)Rsky/?
Ptpn11tm1.1Wbm/Ptpn11tm1.1Wbm
involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 MGI:5588148
cn3
Egr2tm2(cre)Pch/Egr2+
Gt(ROSA)26Sortm8(Map2k1*,EGFP)Rsky/?
Ptpn11tm1.1Wbm/Ptpn11tm1.1Wbm
involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 MGI:5588145
cn4
Egr2tm2(cre)Pch/Egr2+
Ptpn11tm1.1Wbm/Ptpn11tm1.1Wbm
involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL MGI:4365548
cn5
Ptpn11tm1.1Wbm/Ptpn11tm1.1Wbm
H2az2Tg(Wnt1-cre)11Rth/H2az2+
involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * SJL * SJL/J MGI:4365544
cn6
Gt(ROSA)26Sortm7(Pik3ca*,EGFP)Rsky/?
Ptpn11tm1.1Wbm/Ptpn11tm1.1Wbm
Tg(Dhh-cre)1Mejr/0
involves: 129P2/OlaHsd * C57BL/6 * FVB/N MGI:5588151
cn7
Gt(ROSA)26Sortm8(Map2k1*,EGFP)Rsky/?
Ptpn11tm1.1Wbm/Ptpn11tm1.1Wbm
Tg(Dhh-cre)1Mejr/0
involves: 129P2/OlaHsd * C57BL/6 * FVB/N MGI:5588150
cn8
Ptpn11tm1.1Wbm/Ptpn11tm1.1Wbm
Tg(Dhh-cre)1Mejr/0
involves: 129P2/OlaHsd * FVB/N MGI:5588149


Genotype
MGI:4365547
cn1
Allelic
Composition
Ptpn11tm1.1Wbm/Ptpn11tm1.1Wbm
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ptpn11tm1.1Wbm mutation (1 available); any Ptpn11 mutation (46 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• following treatment with His-TAT-NLS-cre, Schwann cells exhibit severely blunted Nrg1-induced proliferation and blocked Nrg1-induced migration compared with similarly treated wild-type cells even in the presence of the Shp2 inhibitor PHPS1




Genotype
MGI:5588148
cn2
Allelic
Composition
Egr2tm2(cre)Pch/Egr2+
Gt(ROSA)26Sortm7(Pik3ca*,EGFP)Rsky/?
Ptpn11tm1.1Wbm/Ptpn11tm1.1Wbm
Genetic
Background
involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Egr2tm2(cre)Pch mutation (2 available); any Egr2 mutation (33 available)
Gt(ROSA)26Sortm7(Pik3ca*,EGFP)Rsky mutation (1 available); any Gt(ROSA)26Sor mutation (993 available)
Ptpn11tm1.1Wbm mutation (1 available); any Ptpn11 mutation (46 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• myelination defects are more pronounced than in single conditional Ptpn11tm1.1Wbm homozygotes




Genotype
MGI:5588145
cn3
Allelic
Composition
Egr2tm2(cre)Pch/Egr2+
Gt(ROSA)26Sortm8(Map2k1*,EGFP)Rsky/?
Ptpn11tm1.1Wbm/Ptpn11tm1.1Wbm
Genetic
Background
involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Egr2tm2(cre)Pch mutation (2 available); any Egr2 mutation (33 available)
Gt(ROSA)26Sortm8(Map2k1*,EGFP)Rsky mutation (1 available); any Gt(ROSA)26Sor mutation (993 available)
Ptpn11tm1.1Wbm mutation (1 available); any Ptpn11 mutation (46 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• mice show normal myelination at P15, however axons of peripheral nerves are hypermyelinated by P90




Genotype
MGI:4365548
cn4
Allelic
Composition
Egr2tm2(cre)Pch/Egr2+
Ptpn11tm1.1Wbm/Ptpn11tm1.1Wbm
Genetic
Background
involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Egr2tm2(cre)Pch mutation (2 available); any Egr2 mutation (33 available)
Ptpn11tm1.1Wbm mutation (1 available); any Ptpn11 mutation (46 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• in the ventral but not dorsal roots
• peripheral nerves are hypomyelinated with thinner myelin in axons with larger axon diameter (J:153219)
• in the saphenous nerve




Genotype
MGI:4365544
cn5
Allelic
Composition
Ptpn11tm1.1Wbm/Ptpn11tm1.1Wbm
H2az2Tg(Wnt1-cre)11Rth/H2az2+
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * SJL * SJL/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
H2az2Tg(Wnt1-cre)11Rth mutation (2 available); any H2az2 mutation (26 available)
Ptpn11tm1.1Wbm mutation (1 available); any Ptpn11 mutation (46 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

nervous system
• at E11.5, cutaneous, intercostal, and limb sensory neuron projections exhibit reduced axonal arborization compared to in wild-type mice
• however, incubation with wild-type Schwann cells restores axon outgrowth
• at E11.5, cutaneous, intercostal, and limb sensory neuron projections exhibit defasciculation unlike in wild-type mice
• Ret+ enteric neural crest cells are reduced compared to in wild-type mice
• at E11.5, BFABP+ Schwann cell precursors are reduced compared to in wild-type mice
• at E12.5, Sox10+ Schwann cell precursors are not detected in peripheral nerves unlike in wild-type mice
• at E13.5, Schwann cell nuclei in peripheral nerves are virtually absent unlike in wild-type mice
• at E11.5, cutaneous, intercostal, and limb sensory neuron projections exhibit defasciculation and reduced axonal arborization compared to in wild-type mice
• at E12.5, lumbar dorsal root ganglia sensory neurons exhibit increased cell death compared to in wild-type mice
• numbers of sensory neurons in the dorsal root ganglia are strongly reduced compared to in wild-type mice

craniofacial

pigmentation
• melanocytes are reduced in number compared to in wild-type mice

embryo
• Ret+ enteric neural crest cells are reduced compared to in wild-type mice

cellular
• at E11.5, cutaneous, intercostal, and limb sensory neuron projections exhibit reduced axonal arborization compared to in wild-type mice
• however, incubation with wild-type Schwann cells restores axon outgrowth
• at E11.5, cutaneous, intercostal, and limb sensory neuron projections exhibit defasciculation unlike in wild-type mice




Genotype
MGI:5588151
cn6
Allelic
Composition
Gt(ROSA)26Sortm7(Pik3ca*,EGFP)Rsky/?
Ptpn11tm1.1Wbm/Ptpn11tm1.1Wbm
Tg(Dhh-cre)1Mejr/0
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gt(ROSA)26Sortm7(Pik3ca*,EGFP)Rsky mutation (1 available); any Gt(ROSA)26Sor mutation (993 available)
Ptpn11tm1.1Wbm mutation (1 available); any Ptpn11 mutation (46 available)
Tg(Dhh-cre)1Mejr mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• mice show myelination defects similar to single conditional Ptpn11tm1.1Wbm homozygotes




Genotype
MGI:5588150
cn7
Allelic
Composition
Gt(ROSA)26Sortm8(Map2k1*,EGFP)Rsky/?
Ptpn11tm1.1Wbm/Ptpn11tm1.1Wbm
Tg(Dhh-cre)1Mejr/0
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gt(ROSA)26Sortm8(Map2k1*,EGFP)Rsky mutation (1 available); any Gt(ROSA)26Sor mutation (993 available)
Ptpn11tm1.1Wbm mutation (1 available); any Ptpn11 mutation (46 available)
Tg(Dhh-cre)1Mejr mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• axons of peripheral nerves are hypermyelinated at P90
• however, mice show normal numbers of Schwann cells




Genotype
MGI:5588149
cn8
Allelic
Composition
Ptpn11tm1.1Wbm/Ptpn11tm1.1Wbm
Tg(Dhh-cre)1Mejr/0
Genetic
Background
involves: 129P2/OlaHsd * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ptpn11tm1.1Wbm mutation (1 available); any Ptpn11 mutation (46 available)
Tg(Dhh-cre)1Mejr mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• disruption of entry into the myelination program of remaining Schwann cells





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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory