Excel File Text File All mouse models of hamartoma syndrome with phenotypic similarity to the human disease
        Disease Term Allelic Composition Genetic Background Reference Phenotypes
      Cowden syndrome 1 Ptentm1Mak/Pten+ involves: 129P2/OlaHsd * C57BL/6J J:63478 View
Cowden syndrome 1 Ptentm1Ppp/Pten+ involves: 129S1/Sv * C57BL/6J J:49532 View
Cowden syndrome 1 Ptentm1Rps/Pten+ involves: 129S1/Sv * C57BL/6J J:53065 View
tuberous sclerosis Myl2tm1(cre)Krc/Myl2+
Tsc1tm1Djk/Tsc1tm1Djk		 involves: 129S4/SvJae J:96138 View
tuberous sclerosis Tg(CMV-Tsc2*)1Arbi/0 involves: C57BL/6 J:96943, J:179850 View
tuberous sclerosis Tg(GFAP-cre)8Gtm/0
Tsc2tm1.1Mjg/Tsc2tm1.1Mjg		 involves: 129X1/SvJ * 129S1/Sv * C57BL/6 * CBA J:167241 View
tuberous sclerosis Tg(Pcp2-cre)2Mpin/0
Tsc2tm1.1Mjg/Tsc2tm1.1Mjg		 involves: 129S1/Sv * 129X1/SvJ * C57BL/6J J:174327 View
tuberous sclerosis Tg(Pcp2-cre)2Mpin/0
Tsc2tm1.1Mjg/Tsc2tm1.2Mjg		 involves: 129S1/Sv * 129X1/SvJ * C57BL/6J J:174327 View
tuberous sclerosis Tsc1tm1.1Djk/Tsc1+ either: 129S4/SvJae-Tsc1tm1Djk or (involves: 129S4/SvJae * BALB/cJ) or (involves: 129S4/SvJae * C57BL/6J) J:75243 View
tuberous sclerosis Tsc1tm1Chdl/Tsc1+ involves: 129P2/OlaHsd * Balb/cOlaHsd * C57BL/6JOlaHsd J:99796 View
tuberous sclerosis Tsc1tm1Chdl/Tsc1+ involves: 129P2/OlaHsd * C3H/HeNHsd * C57BL/6JOlaHsd J:99796 View
tuberous sclerosis Tsc1tm1Chdl/Tsc1+ involves: 129P2/OlaHsd * C57BL/6JOlaHsd J:99796 View
tuberous sclerosis Tsc1tm1Djk/Tsc1tm1.1Djk
Tg(Syn1-cre)671Jxm/0		 involves: 129S4/SvJae * C57BL/6 * CBA J:136366 View
tuberous sclerosis Tsc1tm1Djk/Tsc1tm1Djk
Gt(ROSA)26Sortm1Sho/Gt(ROSA)26Sor+		 involves: 129S4/SvJae * 129S4/SvJaeSor J:221022 View
tuberous sclerosis Tsc1tm1Djk/Tsc1tm1Djk
Tg(GFAP-cre)8Gtm/0		 involves: 129S4/SvJae * C57BL/6 * CBA J:134889, J:167241 View
tuberous sclerosis Tsc1tm1Hin/Tsc1+ B6J.129S4-Tsc1tm1Hin J:221239 View
tuberous sclerosis Tsc1tm1Hin/Tsc1+ involves: 129S4/SvJae * C57BL/6J J:70463 View
tuberous sclerosis Tsc2tm1Djk/Tsc2+ either: (involves: 129S4/SvJae * BALB/cJ) or (involves: 129S4/SvJae * Black Swiss) or (involves: 129S4/SvJae * C57BL/6J) J:57631 View
tuberous sclerosis Tsc2tm1Djk/Tsc2+ involves: 129S4/SvJae * C57BL/6NCrl J:138621 View
tuberous sclerosis Tsc2tm1Tno/Tsc2+ B6J.129S4-Tsc2tm1Tno J:221239 View
tuberous sclerosis Tsc2tm1Tno/Tsc2+ involves: 129S4/SvJae * C57BL/6J J:52464 View
tuberous sclerosis Tsc2tm2.2Djk/Tsc2+ involves: 129S4/SvJae * C57BL/6 J:149326 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
Transgenes and
Other Mutations		     tuberous sclerosis Emx1tm1(cre)Ito/Emx1+
Tg(CAG-Mtor*)#Atai/0		 involves: 129P2/OlaHsd * C57BL/6 * DBA/2 * ICR J:211789 View