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All mouse models of Cowden syndrome with phenotypic similarity to the human disease
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| Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
  | Bannayan-Riley-Ruvalcaba syndrome | Ptentm1Mak/Pten+ | involves: 129P2/OlaHsd * C57BL/6J | J:63478 | View | |||
| Bannayan-Riley-Ruvalcaba syndrome | Ptentm1Ppp/Pten+ | involves: 129S1/Sv * C57BL/6J | J:49532 | View | ||||
| Bannayan-Riley-Ruvalcaba syndrome | Ptentm1Rps/Pten+ | involves: 129S1/Sv * C57BL/6J | J:53065 | View | ||||
| | Cowden syndrome | Ptentm1.1Gle/Pten+ | involves: 129S6/SvEvTac * Black Swiss * FVB/N | J:158751 | View | |||
| Cowden syndrome | Ptentm1.2Mwst/Pten+ | involves: 129S6/SvEvTac * Black Swiss * FVB/N | J:158751 | View | ||||
| Cowden syndrome |
Ptentm1Hwu/Ptentm1Hwu Tg(KRT14-cre)#Smr/0 |
FVB.Cg-Ptentm1Hwu Tg(KRT14-cre)#Smr | J:199362 | View | ||||
| Cowden syndrome |
Ptentm1Hwu/Ptentm1Hwu Tg(KRT14-cre)#Smr/0 |
involves: 129S4/SvJae * C57BL/6J * SJL/J | J:138927 | View | ||||
| Cowden syndrome |
Ptentm1Hwu/Ptentm1Hwu Tg(MMTV-cre)4Mam/0 |
involves: 129S4/SvJae * FVB | J:78415 | View | ||||
| Cowden syndrome |
Ptentm1Hwu/Ptentm1Hwu Tg(Mx1-cre)1Cgn/0 |
involves: 129S4/SvJae * C57BL/6 * CBA | J:118329 | View | ||||
| Cowden syndrome | Ptentm1Mak/Pten+ | involves: 129P2/OlaHsd * C57BL/6J | J:63478 | View | ||||
| Cowden syndrome | Ptentm1Ppp/Pten+ | involves: 129S1/Sv * C57BL/6J | J:49532 | View | ||||
| Cowden syndrome | Ptentm1Rps/Pten+ | involves: 129S1/Sv * C57BL/6J | J:53065 | View | ||||
| Cowden syndrome | Ptentm2.1Gle/Pten+ | involves: 129S6/SvEvTac * Black Swiss * FVB/N | J:158751 | View | ||||
| Cowden syndrome |
Ptentm2Mak/Ptentm2Mak Tg(Gfap-cre)1Sbk/0 |
involves: 129P2/OlaHsd | J:75500 | View | ||||
| Cowden syndrome |
Ptentm2Mak/Ptentm2Mak Tg(Nes-cre/ERT2,-ALPP)1Sbk/0 |
involves: 129P2/OlaHsd | J:237990 | View | ||||