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All mouse models of Prader-Willi syndrome with phenotypic similarity to the human disease
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| Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
  | Prader-Willi syndrome | Del(7Herc2-Mkrn3)13FRdni/+ | involves: C57BL/6 * CD-1 * SJL | J:56614 | View | |||
| Prader-Willi syndrome | Ndntm1.1Mus/Ndn+ | B6.129S2-Ndntm1.1Mus | J:119656 | View | ||||
| Prader-Willi syndrome | Ndntm1.1Mus/Ndn+ | involves: 129S2/SvPas * C57BL/6J | J:66557 | View | ||||
| Prader-Willi syndrome | Ndntm1Ky/Ndn+ | involves: C57BL/6 * CBA * ICR/Slc | J:100024 | View | ||||
| Prader-Willi syndrome | Ndntm1Stw/Ndn+ | involves: 129S1/Sv * C57BL/6 | J:57890 | View | ||||
| Prader-Willi syndrome | Ndntm1Stw/Ndn+ | involves: 129S1/Sv * FVB | J:57890 | View | ||||
| Prader-Willi syndrome | Ndntm2Stw/Ndn+ | involves: 129S1/Sv * C57BL/6 | J:57890 | View | ||||
| Prader-Willi syndrome | Ndntm2Stw/Ndn+ | involves: 129S1/Sv * C57BL/6J | J:82266 | View | ||||
| Prader-Willi syndrome | Snrpntm1Rsnk/Snrpn+ | either: 129S1-Snrpntm1Rsnk or (involves: 129S1/Sv * C57BL/6J) | J:105412 | View | ||||
| Prader-Willi syndrome | Snrpntm2Alb/Snrpn+ | involves: 129S7/SvEvBrd * C57BL/6J | J:70275 | View | ||||
| Prader-Willi syndrome | Snrpntm2Cbr/Snrpn+ | involves: 129S1/Sv * C57BL/6 | J:47318 | View | ||||
| | Prader-Willi syndrome | Htr2ctm1.1Eme/Y | involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 | J:163043 | View | |||
| Prader-Willi syndrome | Magel2tm1Stw/Magel2+ | C57BL/6-Magel2tm1Stw | J:144836 | View | ||||
| Prader-Willi syndrome | Magel2tm1Stw/Magel2tm1Stw | C57BL/6-Magel2tm1Stw/J | J:233299 | View | ||||
| Transgenes and Other Mutations | Prader-Willi syndrome | Del(7Ipw-Snord116)1Jbro/+ | involves: 129S7/SvEvBrd * C57BL/6 | J:242655 | View | |||
| Prader-Willi syndrome | Snord116tm1.1Uta/Snord116+ | involves: C57BL/6J | J:131427 | View | ||||
| Prader-Willi syndrome |
Snord116tm1Uta/Snord116+ Tg(Zp3-cre)93Knw/0 |
involves: C57BL/6J | J:131427 | View | ||||
| Prader-Willi syndrome | T(7;18)50H/+ | involves: 101/H * C3H/HeH | J:3618 | View | ||||
| Prader-Willi syndrome | T(7;18)50H/+ | involves: 101/H * C3H/HeH | J:3618 | View | ||||
| Prader-Willi syndrome | Tg(Igh-Lmp2a)13FRdni/0 | involves: C57BL/6 * CD-1 * SJL | J:56614 | View | ||||
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No similarity to the expected human disease phenotype was found.
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| Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
| NOT Models | Prader-Willi syndrome |
Frat1tm1Brn/Frat1tm1Brn Frat2tm2Brn/Frat2tm2Brn Peg12tm1Brn/Peg12tm1Brn |
involves: 129P2/OlaHsd * FVB | J:96034 | View | |||
| Prader-Willi syndrome | Ndntm1Alb/Ndn+ | involves: 129S7/SvEvBrd | J:55267 | View | ||||
| Prader-Willi syndrome | Ndntm1Alb/Ndntm1Alb | involves: 129S7/SvEvBrd | J:55267 | View | ||||
| Prader-Willi syndrome | Peg12tm1Brn/Peg12tm1Brn | involves: 129P2/OlaHsd * FVB | J:96034 | View | ||||