![]() ![]() |
||||||||
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 |