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All mouse models of GM2 gangliosidosis with phenotypic similarity to the human disease
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| Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
  | GM2 gangliosidosis, AB variant | \Gm2atm1Rlp/\Gm2atm1Rlp | involves: 129S4/SvJae * C57BL/6 | J:41950 | View | |||
| Sandhoff disease |
\Ccl3tm1Unc/\Ccl3+ \Hexbtm1Rlp/\Hexbtm1Rlp |
involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 | J:90687 | View | ||||
| Sandhoff disease |
\Ccl3tm1Unc/\Ccl3tm1Unc \Hexbtm1Rlp/\Hexbtm1Rlp |
involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 | J:90687 | View | ||||
| Sandhoff disease |
\Fcer1gtm1Rav/\Fcer1gtm1Rav \Hexbtm1Rlp/\Hexbtm1Rlp |
involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 | J:87617 | View | ||||
| Sandhoff disease | \Hexblysd/\Hexblysd | B6.Cg-Hexblysd/J | J:301674 | View | ||||
| Sandhoff disease | \Hexbtm1Grv/\Hexbtm1Grv | either: (involves: 129P2/Ola * C57BL/6J) or (involves: 129S1/Sv * 129X1/SvJ * C57L/6J) | J:30899 | View | ||||
| Sandhoff disease | \Hexbtm1Rlp/\Hexbtm1Rlp | involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 | J:87617 | View | ||||
| Sandhoff disease | \Hexbtm1Rlp/\Hexbtm1Rlp | involves: 129S4/SvJae * C57BL/6 | J:29268, J:190450 | View | ||||
| Sandhoff disease |
\Hexbtm1Rlp/\Hexbtm1Rlp \Tg(Hexb-tTA2S,tetO-Hexb)#Tjsa/0 |
involves: 129S4/SvJae * C57BL/6 * CBA | J:190450 | View | ||||
| Sandhoff disease |
\Hexbtm1Rlp/\Hexbtm1Rlp \Tg(SYN1-tTA2S,tetO-Hexb)#Tjsa/0 |
involves: 129S4/SvJae * C57BL/6 * CBA | J:190450 | View | ||||
| Tay-Sachs disease | \Hexatm1Cota/\Hexatm1Cota | involves: 129S2/SvPas * C57BL/6 | J:30435 | View | ||||
| Tay-Sachs disease | \Hexatm1Grv/\Hexatm1Grv | involves: 129P2/Ola * C57BL/6J | J:30899 | View | ||||
| Tay-Sachs disease | \Hexatm1Rlp/\Hexatm1Rlp | involves: 129S4/SvJae * C57BL/6 | J:21008 | View | ||||