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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(Myh7-Ptpn11*Q79R)11Rbns
transgene insertion 11, Jeffrey Robbins
MGI:3822132
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cx1
Mapk3tm1Gpg/Mapk3tm1Gpg
Tg(Myh7-Ptpn11*Q79R)11Rbns/0
involves: 129/Sv * FVB/N MGI:3822148
cx2
Mapk1tm1Melo/Mapk1+
Tg(Myh7-Ptpn11*Q79R)11Rbns/0
involves: 129S2/SvPas * FVB/N MGI:3822149
tg3
Tg(Myh7-Ptpn11*Q79R)11Rbns/0 FVB.Cg-Tg(Myh7-Ptpn11*Q79R)11Rbns MGI:3822143


Genotype
MGI:3822148
cx1
Allelic
Composition
Mapk3tm1Gpg/Mapk3tm1Gpg
Tg(Myh7-Ptpn11*Q79R)11Rbns/0
Genetic
Background
involves: 129/Sv * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mapk3tm1Gpg mutation (1 available); any Mapk3 mutation (26 available)
Tg(Myh7-Ptpn11*Q79R)11Rbns mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
N
• unlike in Tg(Myh7-Ptpn11*Q79R)11Rbns mice, heart weight, ventricular compaction, cardiac cell proliferation and heart function are normal

respiratory system
N
• unlike in Tg(Myh7-Ptpn11*Q79R)11Rbns mice, lung weight is normal




Genotype
MGI:3822149
cx2
Allelic
Composition
Mapk1tm1Melo/Mapk1+
Tg(Myh7-Ptpn11*Q79R)11Rbns/0
Genetic
Background
involves: 129S2/SvPas * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mapk1tm1Melo mutation (0 available); any Mapk1 mutation (43 available)
Tg(Myh7-Ptpn11*Q79R)11Rbns mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
N
• unlike in Tg(Myh7-Ptpn11*Q79R)11Rbns mice, heart weight, ventricular compaction, cardiac cell proliferation and heart function are normal

respiratory system
N
• unlike in Tg(Myh7-Ptpn11*Q79R)11Rbns mice, lung weight is normal




Genotype
MGI:3822143
tg3
Allelic
Composition
Tg(Myh7-Ptpn11*Q79R)11Rbns/0
Genetic
Background
FVB.Cg-Tg(Myh7-Ptpn11*Q79R)11Rbns
Find Mice Using the International Mouse Strain Resource (IMSR)
No mouse lines available in IMSR.
See publication links below for author information.
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• 39% of mice die by 8 months of age

cardiovascular system
• postmortem
• at E16.5, mice exhibit ventricular noncompaction unlike in wild-type mice that persists postnatally without fibrosis
• cells in the noncompacted ventricle exhibit increased proliferation compared to in wild-type mice
• cells in the noncompacted ventricle and located at the boundaries of the muscular ventricular septum and atrioventricular cushion tissue exhibit increased proliferation compared to in wild-type mice

respiratory system

homeostasis/metabolism
• postmortem, mice display chronic left atria thrombi unlike in wild-type mice

muscle

growth/size/body

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Noonan syndrome 1 DOID:0060578 OMIM:163950
J:123963





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