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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Erbb3tm3Cbm
targeted mutation 3, Carmen Birchmeier
MGI:3835516
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Erbb3tm2Cbm/Erbb3tm3Cbm
Erbb4tm1Fej/Erbb4tm1Fej
Cnptm1(cre)Kan/?
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ MGI:3835562
cn2
Erbb3tm3Cbm/Erbb3tm3Cbm
Gt(ROSA)26Sortm8(Map2k1*,EGFP)Rsky/?
Tg(Dhh-cre)1Mejr/0
involves: 129P2/OlaHsd * C57BL/6 * FVB/N MGI:5588163
cn3
Erbb3tm3Cbm/Erbb3tm3Cbm
Gt(ROSA)26Sortm7(Pik3ca*,EGFP)Rsky/?
Tg(Dhh-cre)1Mejr/0
involves: 129P2/OlaHsd * C57BL/6 * FVB/N MGI:5588164
cn4
Erbb3tm3Cbm/Erbb3tm3Cbm
Tg(Dhh-cre)1Mejr/0
involves: 129P2/OlaHsd * FVB/N MGI:5588162


Genotype
MGI:3835562
cn1
Allelic
Composition
Erbb3tm2Cbm/Erbb3tm3Cbm
Erbb4tm1Fej/Erbb4tm1Fej
Cnptm1(cre)Kan/?
Genetic
Background
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cnptm1(cre)Kan mutation (0 available); any Cnp mutation (27 available)
Erbb3tm2Cbm mutation (0 available); any Erbb3 mutation (48 available)
Erbb3tm3Cbm mutation (0 available); any Erbb3 mutation (48 available)
Erbb4tm1Fej mutation (1 available); any Erbb4 mutation (87 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• develop to term but die in the second post natal week

nervous system
N
• central nervous system myelination is normal up to 11 days of age (optic nerve and corpus callosum)
• severely defective myelination in the peripheral nervous system




Genotype
MGI:5588163
cn2
Allelic
Composition
Erbb3tm3Cbm/Erbb3tm3Cbm
Gt(ROSA)26Sortm8(Map2k1*,EGFP)Rsky/?
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:
Erbb3tm3Cbm mutation (0 available); any Erbb3 mutation (48 available)
Gt(ROSA)26Sortm8(Map2k1*,EGFP)Rsky mutation (1 available); any Gt(ROSA)26Sor mutation (993 available)
Tg(Dhh-cre)1Mejr mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• at P15, the myelin of peripheral axons is thinner but axons are hypermyelinated at P90
• at P15 and P90, 36.7% and 17.8% of axons with diameters >1 um are nonmyelinated, respectively compared to 3.5% and 0.8% in controls
• axons are hypermyelinated at P90
• however, mice show rescue of Schwann cell development and Schwan cells are able to myelinate




Genotype
MGI:5588164
cn3
Allelic
Composition
Erbb3tm3Cbm/Erbb3tm3Cbm
Gt(ROSA)26Sortm7(Pik3ca*,EGFP)Rsky/?
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:
Erbb3tm3Cbm mutation (0 available); any Erbb3 mutation (48 available)
Gt(ROSA)26Sortm7(Pik3ca*,EGFP)Rsky mutation (1 available); any Gt(ROSA)26Sor mutation (993 available)
Tg(Dhh-cre)1Mejr mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• myelination is not seen




Genotype
MGI:5588162
cn4
Allelic
Composition
Erbb3tm3Cbm/Erbb3tm3Cbm
Tg(Dhh-cre)1Mejr/0
Genetic
Background
involves: 129P2/OlaHsd * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Erbb3tm3Cbm mutation (0 available); any Erbb3 mutation (48 available)
Tg(Dhh-cre)1Mejr mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• almost complete absence of Schwann cells





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last database update
11/19/2024
MGI 6.24
The Jackson Laboratory