Excel File Text File All mouse models of Noonan syndrome 1 with phenotypic similarity to the human disease
        Disease Term Allelic Composition Genetic Background Reference Phenotypes
      Noonan syndrome 1 Emx1tm1(cre)Krj/Emx1+
Ptpn11tm6Bgn/Ptpn11+
B6.129S-Ptpn11tm6Bgn Emx1tm1(cre)Krj J:242312 View
Noonan syndrome 1 Ptpn11tm1Bgn/Ptpn11+ involves: 129S4/SvJae * C57BL/6J J:91609 View
Noonan syndrome 1 Tg(Myh7-Ptpn11*Q79R)11Rbns/0 FVB.Cg-Tg(Myh7-Ptpn11*Q79R)11Rbns J:123963 View
Transgenes and
Other Mutations
     Noonan syndrome 1 H2az2Tg(Wnt1-cre)11Rth/H2az2+
Tg(CAG-cat,-Ptpn11*Q97R)1Rbns/0
involves: C57BL/6J * CBA/J * FVB/N J:153094 View
Noonan syndrome 1 Tg(CAG-cat,-Ptpn11*Q97R)1Rbns/0
Tg(Tek-cre)12Flv/0
involves: C3H * C57BL/6 * FVB/N J:142212 View


       
No similarity to the expected human disease phenotype was found.
        Disease Term Allelic Composition Genetic Background Reference Phenotypes
NOT Models      Noonan syndrome 1 Ptpn11tm1Paw/Ptpn11tm1Paw involves: 129S1/Sv * 129X1/SvJ * CD-1 J:43740 View
Noonan syndrome 1 Ptpn11tm1Rbn/Ptpn11+ involves: 129 * Black Swiss J:35137 View
Noonan syndrome 1 Ptpn11tm1Rbn/Ptpn11tm1Rbn involves: 129 * Black Swiss J:35137 View