Excel File Text File All mouse models of Noonan syndrome 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
Noonan syndrome 3 Krastm4.1Bbd/Krastm4.1Bbd involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * C57BL/6J * FVB/N J:223433 View
Noonan syndrome 4 Sos1tm1.2Rak/Sos1+ involves: 129S/Sv * C57BL/6 * FVB/N * SJL J:171873 View
Noonan syndrome 4 Sos1tm1.2Rak/Sos1tm1.2Rak involves: 129S/Sv * C57BL/6 * FVB/N * SJL J:171873 View
Noonan syndrome 5 Raf1tm1.1Bgn/Raf1+ involves: 129S6/SvEvTac * C57BL/6NCr J:172034 View
Noonan syndrome 5 Raf1tm2.1Ara/Raf1tm2.1Ara involves: 129S6/SvEvTac * C57BL/6NCr J:189143 View
Noonan syndrome 8 Rit1tm1.1Tumg/Rit1+ B6.Cg-Rit1tm1.1Tumg J:277548 View
Noonan syndrome 10 Lztr1tm1a(EUCOMM)Wtsi/Lztr1+ involves: C57BL/6N J:268690 View
      Noonan syndrome Apaf1Gt(IRESBetageo)XIX18Pgr/Apaf1Gt(IRESBetageo)XIX18Pgr involves: 129S1/Sv * 129X1/SvJ * NMRI J:49840 View
Noonan syndrome Kat6bGt(pKC199)1Pgr/Kat6bGt(pKC199)1Pgr involves: 129S2/SvPas J:178264 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