Excel File Text File All mouse models of physical disorder with phenotypic similarity to the human disease
        Disease Term Allelic Composition Genetic Background Reference Phenotypes
      alacrima, achalasia, and impaired intellectual development syndrome Gmppatm1d(EUCOMM)Wtsi/Gmppatm1d(EUCOMM)Wtsi involves: C57BL/6N J:305791 View
atrial heart septal defect 2 Gata4tm1Grg/Gata4+ involves: 129 * C57BL/6 J:185124 View
atrial heart septal defect 7 Nkx2-5tm2.1Mwc/Nkx2-5+ B6J.Cg-Nkx2-5tm2.1Mwc/Mwc J:239808 View
atrial heart septal defect 7 Nkx2-5tm3.1Mwc/Nkx2-5+ B6J.Cg-Nkx2-5tm3.1Mwc/Mwc J:239808 View
autosomal dominant congenital deafness with onychodystrophy Atp6v1b2tm1Yoyu/Atp6v1b2+ involves: C57BL/6 J:278514 View
autosomal dominant congenital deafness with onychodystrophy Atp6v1b2tm1Yoyu/Atp6v1b2tm1Yoyu involves: C57BL/6 J:278514 View
autosomal recessive congenital ichthyosis 1 Tgm1tm1Kfyn/Tgm1tm1Kfyn involves: 129S1/SvImJ * 129X1/SvJ * C57BL/6 J:45653, J:74334 View
autosomal recessive congenital ichthyosis 4B Abca12el12/Abca12el12 involves: 129/Sv * C57BL/6 J:161652 View
autosomal recessive congenital ichthyosis 4B Abca12smsk/Abca12smsk involves: C57BL/6J J:262458 View
autosomal recessive congenital ichthyosis 4B Abca12tm1Lex/Abca12tm1Lex involves: 129S/SvEvBrd * C57BL/6J J:144062 View
autosomal recessive congenital ichthyosis 4B Abca12tm1Shzu/Abca12tm1Shzu B6.129S-Abca12tm1Shzu J:139048 View
autosomal recessive congenital ichthyosis 10 Pnpla1tm1a(KOMP)Wtsi/Pnpla1tm1a(KOMP)Wtsi B6NTac;B6N-Atm1Brd Pnpla1tm1a(KOMP)Wtsi/Ics J:242353 View
autosomal recessive congenital ichthyosis 13 Sdr9c7em1Maak/Sdr9c7em1Maak involves: C57BL/6J J:295441 View
Bethlem myopathy Col6a1tm1Gmb/Col6a1tm1Gmb involves: 129S1/Sv * 129X1/SvJ * C57BL/6 J:51410, J:86734 View
buphthalmos Cyp1b1tm1Gonz/Cyp1b1tm1Gonz 129X1.Cg-Cyp1b1tm1Gonz J:82280 View
buphthalmos Cyp1b1tm1Gonz/Cyp1b1tm1Gonz B6.Cg-Cyp1b1tm1Gonz J:82280 View
buphthalmos Cyp1b1tm1Gonz/Cyp1b1tm1Gonz involves: 129X1/SvJ * C57BL/6J J:82280 View
buphthalmos Cyp1b1tm1Gonz/Cyp1b1tm1Gonz
Tyrc-2J/Tyrc-2J		 B6.Cg-Tyrc-2J Cyp1b1tm1Gonz J:82280 View
Char syndrome Tfap2btm1Rbu/Tfap2btm1Rbu involves: 129S1/Sv * 129X1/SvJ J:175832 View
cleft lip Irf6tm1Bcsl/Irf6tm1Bcsl
Pitx2tm4(cre)Jfm/Pitx2+		 involves: 129 J:275989 View
Compton-North congenital myopathy Cntn1m1J/Cntn1m1J B6;C-Cntn1m1J/GrsrJ J:222308 View
Compton-North congenital myopathy Cntn1usl/Cntn1usl B6.MRL-Cntn1usl/GrsrJ J:222308 View
Compton-North congenital myopathy Cntn1usl/Cntn1usl MRL/MpJ-Faslpr Cntn1usl/GrsrJ J:222308 View
congenital adrenal hyperplasia Cyp11b1tm1Chjk/Cyp11b1tm1Chjk involves: 129P2/OlaHsd * C57BL/6J J:147610 View
congenital adrenal hyperplasia Startm1Klp/Startm1Klp involves: 129P2/OlaHsd J:43589, J:55588, J:64337 View
congenital afibrinogenemia Fggtm1Fjc/Fggtm1Fjc involves: 129S1/Sv * 129X1/SvJ * C57BL/6 J:75302 View
congenital bile acid synthesis defect 5 Abcd3tm1Safe/Abcd3tm1Safe involves: 129S4/SvJae * C57BL/6J J:217065 View
congenital central hypoventilation syndrome Phox2btm1Rth/Phox2b+
Hprt1tm1(CAG-cre)Mnn/?		 involves: 129 * 129S1/Sv * C57BL/6 J:331513 View
congenital central hypoventilation syndrome Phox2btm2Jbr/Phox2b+ involves: 129S2/SvPas * C57BL/6 J:131365 View
congenital diaphragmatic hernia Frem1eyes2/Frem1eyes2 involves: 129S6/SvEvTac * C57BL/6J J:192553 View
congenital diaphragmatic hernia Pls3em1Bult/Pls3em1Bult C57BL/6J-Pls3em1Bult/BultJ J:341714 View
congenital diaphragmatic hernia Pls3em1Bult/Y C57BL/6J-Pls3em1Bult/BultJ J:341714 View
congenital diaphragmatic hernia Zfpm2lil/Zfpm2lil involves: A/J J:100119 View
congenital diarrhea 5 with tufting enteropathy EpcamGt(RST412)Byg/EpcamGt(RST412)Byg involves: 129P2/OlaHsd * C57BL/6 J:195002 View
congenital disorder of glycosylation type IIa Mgat2tm1.1Jxm/Mgat2tm1.1Jxm involves: 129S1/Sv * 129X1/SvJ * C57BL/6 J:80661 View
congenital disorder of glycosylation type IIa Mgat2tm1.1Jxm/Mgat2tm1.1Jxm involves: 129S1/Sv * 129X1/SvJ * ICR J:80661 View
congenital disorder of glycosylation type IIc Slc35c1tm1Cknr/Slc35c1tm1Cknr involves: 129/Sv * 129P2/OlaHsd * C57BL/6 J:121151 View
congenital generalized lipodystrophy type 1 Agpat2tm1Garg/Agpat2tm1Garg involves: 129S6/SvEvTac J:146649 View
congenital generalized lipodystrophy type 2 Bscl2tm1.1Lchan/Bscl2tm1.1Lchan involves: 129S1/Sv * 129X1/SvJ * C57BL/6J J:211142 View
congenital generalized lipodystrophy type 2 Bscl2tm1.2Gliu/Bscl2tm1.2Gliu involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/N J:173404, J:211072 View
congenital generalized lipodystrophy type 2 Bscl2tm1Geno/Bscl2tm1Geno B6.129P2-Bscl2tm1Geno J:200947 View
congenital generalized lipodystrophy type 4 Cavin1tm1Pfp/Cavin1tm1Pfp involves: 129S6/SvEvTac * C57BL/6 J:150419 View
congenital heart disease Nkx2-5tm1.1Burg/Nkx2-5+ involves: 129S1/Sv * 129S2/SvPasCrl * 129X1/SvJ J:251389 View
congenital heart disease Nkx2-5tm1.1Hkas/Nkx2-5+ 129S2.Cg-Nkx2-5tm1.1Hkas J:273096, J:273097 View
congenital hereditary endothelial dystrophy of cornea Slc4a11tm1.1Jrcy/Slc4a11tm1.1Jrcy involves: C57BL/6 J:214272 View
congenital hypothyroidism Duox2thyd/Duox2thyd B6(129)-Duox2thyd/J J:121821 View
congenital hypothyroidism Pax8tm1(cre)Mbu/Pax8tm1(cre)Mbu involves: 129P2/OlaHsd * C3H/He * C57BL/6 J:80208 View
congenital hypothyroidism Pax8tm1Pgr/Pax8tm1Pgr either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) J:47310, J:116236 View
congenital hypothyroidism Pax8tm1Pgr/Pax8tm1Pgr involves: 129S1/Sv * 129X1/SvJ J:130062 View
congenital hypothyroidism TpoR479C/TpoR479C involves: ICR J:112930 View
congenital megabladder Myocdem1Blk/Myocdtm1.1Msp involves: 129 J:283803 View
congenital megabladder Myocdtm1.1Msp/mgb involves: 129/Sv * FVB/N J:283803 View
congenital merosin-deficient muscular dystrophy 1A Lama2dy-2J/Lama2dy-2J B6.WK-Lama2dy-2J J:97464 View
congenital merosin-deficient muscular dystrophy 1A Lama2dy-6J/Lama2dy-6J involves: C57BL/6JEi * DBA/2J J:56803 View
congenital merosin-deficient muscular dystrophy 1A Lama2dy-7J/Lama2dy-7J C57BL/6J-Lama2dy-7J/J J:134367 View
congenital merosin-deficient muscular dystrophy 1A Lama2dy-8J/Lama2dy-8J C57BL/6J-Lama2dy-8J/GrsrJ J:149729 View
congenital merosin-deficient muscular dystrophy 1A Lama2dy-Pas/Lama2dy-Pas involves: non-inbred stock J:102806 View
congenital merosin-deficient muscular dystrophy 1A Lama2dy/Lama2dy involves: 129P1/Re J:13125 View
congenital merosin-deficient muscular dystrophy 1A Lama2tm1Eeng/Lama2tm1Eeng involves: 129S1/Sv J:170192 View
congenital merosin-deficient muscular dystrophy 1A Lama2tm1Eeng/Lama2tm1Eeng involves: 129S1/Sv * Black Swiss J:59089 View
congenital merosin-deficient muscular dystrophy 1A Lama2tm1Eeng/Lama2tm1Eeng involves: 129S1/Sv * Black Swiss * FVB/N J:49435 View
congenital merosin-deficient muscular dystrophy 1A Lama2tm1Stk/Lama2tm1Stk involves: 129/Sv * 129P2/OlaHsd * BALB/c * ICR J:43145, J:167230 View
congenital muscular dystrophy due to integrin alpha-7 deficiency Itga7tm1Umr/Itga7tm1Umr involves: 129S1/Sv * 129X1/SvJ * C57BL/6 J:82116 View
congenital muscular dystrophy due to LMNA mutation Lmnatm2.1Gbon/Lmnatm2.1Gbon involves: 129 * C57BL/6 J:180603 View
congenital myasthenic syndrome 4C Chrnetm1Vwi/Chrnetm1Vwi involves: 129P2/OlaHsd * C57BL/6 J:128178 View
congenital myasthenic syndrome 5 Colqtm1Jrs/Colqtm1Jrs involves: 129S1/Sv * 129X1/SvJ J:54006 View
congenital myasthenic syndrome 6 Chattm1.1Jrs/Chattm1.1Jrs Not Specified J:91066 View
congenital myasthenic syndrome 6 Chattm1Fhg/Chattm1Fhg involves: 129S2/SvPas * C57BL/6 J:81738 View
congenital myasthenic syndrome 8 Agrnnmf380/Agrnnmf380 C57BL/6J-Agrnnmf380/J J:176117 View
congenital myasthenic syndrome 9 Musktm1.1Vwi/Musktm2Vwi Not Specified J:141024 View
congenital myasthenic syndrome 9 Musktm1Vwi/Musktm1.1Vwi
Tg(Ckmm-cre)5Khn/0		 involves: C57BL/6J * FVB J:106867 View
congenital myasthenic syndrome 9 Musktm1Vwi/Musktm1Vwi
Tg(Ckmm-cre)5Khn/0		 involves: C57BL/6J * FVB J:106867 View
congenital myasthenic syndrome 10 Dok7tm2Yyam/Dok7tm2Yyam involves: 129P2/OlaHsd * C57BL/6J J:213767 View
congenital myasthenic syndrome 11 Rapsnem1Gan/Rapsnem1Gan C57BL/6J-Rapsnem1Gan J:282816 View
congenital myasthenic syndrome 12 Gfpt1tm1c(EUCOMM)Wtsi/Gfpt1tm1c(EUCOMM)Wtsi
Tg(Ckmm-cre)5Khn/0		 involves: C57BL/6J * C57BL/6N * SJL/J J:265013 View
congenital myasthenic syndrome 19 Col13a1tm3.1Pih/Col13a1tm3.1Pih involves: 129S1/Sv * 129X1/SvJ J:242846 View
congenital nonspherocytic hemolytic anemia Gpi1b-m1Neu/Gpi1b-m1Neu C3.Cg-Gpi1b-m1Neu J:35956 View
congenital nonspherocytic hemolytic anemia Gpi1b-m2Neu/Gpi1b-m2Neu C3.Cg-Gpi1b-m2Neu J:35956 View
congenital nystagmus 1 Frmd7tm1b(KOMP)Wtsi/Frmd7tm1b(KOMP)Wtsi involves: C57BL/6 * C57BL/6N J:299010 View
congenital nystagmus 1 Frmd7tm1b(KOMP)Wtsi/Y involves: C57BL/6 * C57BL/6N J:299010 View
congenital secretory chloride diarrhea 1 Slc26a3tm1Sole/Slc26a3tm1Sole involves: 129S6/SvEvTac * C57BL/6 J:117587 View
congenital stationary night blindness 1A Nyxnob/Nyxnob BALB/c-Nyxnob J:50824 View
congenital stationary night blindness 1B Grm6nob7/Grm6nob7 C57BL/6J-Grm6nob7 J:229885 View
congenital stationary night blindness 1B Grm6nob8/Grm6nob8 CBA/CaJ J:240996 View
congenital stationary night blindness 1D Slc24a1tm1Xen/Slc24a1tm1Xen involves: C57BL/6 J:226323 View
congenital stationary night blindness 1E Gpr179nob5/Gpr179nob5 involves: C3H J:185567 View
congenital stationary night blindness 1F Lrit3tm1Lex/Lrit3tm1Lex involves: 129S5/SvEvBrd * C57BL/6 J:214644 View
congenital stationary night blindness 2A Cacna1fnob2/Cacna1fnob2 AXB6/PgnJ J:123811 View
congenital stationary night blindness 2A Cacna1fnob2/Y AXB6/PgnJ J:123811 View
congenital stationary night blindness 2A Cacna1fnob9/Cacna1fnob9 B6(PWD)-Cacna1fnob9/BocJ J:267160 View
congenital stationary night blindness 2A Cacna1ftm1.1Sdie/Cacna1f+ involves: C57BL/6 J:206214 View
congenital stationary night blindness 2A Cacna1ftm1.1Sdie/Cacna1ftm1.1Sdie B6.Cg-Cacna1ftm1.1Sdie/J J:212726 View
congenital stationary night blindness 2A Cacna1ftm1.1Sdie/Cacna1ftm1.1Sdie involves: C57BL/6 J:206214 View
congenital stationary night blindness 2A Cacna1ftm1.1Sdie/Y B6.Cg-Cacna1ftm1.1Sdie/J J:212726 View
congenital stationary night blindness 2A Cacna1ftm1.1Sdie/Y involves: C57BL/6 J:206214 View
congenital stationary night blindness 2A Cacna1ftm1.2Sdie/Cacna1ftm1.2Sdie B6.Cg-Cacna1ftm1.2Sdie/J J:212726 View
congenital stationary night blindness 2A Cacna1ftm1.2Sdie/Y B6.Cg-Cacna1ftm1.2Sdie/J J:212726 View
congenital stationary night blindness 2A Cacna1ftm1Ntbh/Cacna1ftm1Ntbh B6.129-Cacna1ftm1Ntbh J:102753 View
congenital stationary night blindness 2A Cacna1ftm1Ntbh/Y B6.129-Cacna1ftm1Ntbh J:102753 View
congenital stationary night blindness autosomal dominant 2 Pde6batrd1/Pde6batrd1 involves: BALB/cAnN * C3H/HeN J:75964 View
congenital stationary night blindness autosomal dominant 2 Pde6batrd1/Pde6brd1 involves: BALB/cAnN * C3H/HeN J:75964 View
congenital stationary night blindness autosomal dominant 2 Pde6batrd2/Pde6batrd2 involves: BALB/cAnN * C3H/HeN J:75964 View
congenital stationary night blindness autosomal dominant 2 Pde6batrd2/Pde6brd1 involves: BALB/cAnN * C3H/HeN J:75964 View
congenital stationary night blindness autosomal dominant 2 Pde6batrd3/Pde6batrd3 involves: BALB/cAnN * C3H/HeN J:75964 View
congenital stationary night blindness autosomal dominant 2 Pde6batrd3/Pde6brd1 involves: BALB/cAnN * C3H/HeN J:75964 View
congenital stationary night blindness autosomal dominant 2 Pde6brd1-1H/Pde6brd1 involves: BALB/cAnN * C3H/HeN J:75964 View
congenital stationary night blindness autosomal dominant 2 Pde6brd1-2H/Pde6brd1 involves: BALB/cAnN * C3H/HeN J:75964 View
congenital stationary night blindness autosomal dominant 2 Pde6brd1-2J/Pde6brd1-2J C57BL/6J-Pde6brd1-2J/J J:82238 View
congenital stationary night blindness autosomal dominant 2 Pde6brd1-3H/Pde6brd1-3H involves: BALB/cAnN * C3H/HeN J:75964 View
congenital stationary night blindness autosomal dominant 2 Pde6brd1-3H/Pde6brd1 involves: BALB/cAnN * C3H/HeN J:75964 View
congenital stationary night blindness autosomal dominant 2 Pde6brd1-4H/Pde6brd1-4H involves: BALB/cAnN * C3H/HeN J:75964 View
congenital stationary night blindness autosomal dominant 2 Pde6brd1-4H/Pde6brd1 involves: BALB/cAnN * C3H/HeN J:75964 View
congenital stationary night blindness autosomal dominant 2 Pde6brd1/Pde6brd1 Not Specified J:24999 View
Diamond-Blackfan anemia 6 Rpl5Skax23-Jus/Rpl5+ 129S6.B6-Rpl5Skax23-Jus J:330162 View
Diamond-Blackfan anemia 7 Ndor1Tg(UBC-cre/ERT2)1Ejb/Ndor1+
Rpl11tm1.1Srn/Rpl11+		 involves: 129S6/SvEvTac * C57BL/6NCrl * CD-1 J:292575 View
Fanconi anemia complementation group A Fancatm1.1Wong/Fancatm1.1Wong involves: C57BL/6 J:85108 View
Fanconi anemia complementation group A Fancatm1Faw/Fancatm1Faw involves: 129P2/OlaHsd * FVB J:63742 View
Fanconi anemia complementation group A Fancatm1Wong/Fancatm1Wong involves: C57BL/6 J:85108 View
Fanconi anemia complementation group C Fancctm1Mab/Fancctm1Mab involves: 129S1/Sv * 129X1/SvJ * C57BL/6J J:32080 View
Fanconi anemia complementation group C Fancctm1Mgo/Fancctm1Mgo involves: 129S4/SvJaeSor * C57BL/6 J:61512 View
Fanconi anemia complementation group D1 Brca2tm1Kamc/Brca2tm1Kamc involves: 129P2/OlaHsd * BALB/c J:144998 View
Fanconi anemia complementation group D2 Aldh2tm1a(EUCOMM)Wtsi/Aldh2tm1a(EUCOMM)Wtsi
Fancd2tm1Hou/Fancd2tm1Hou		 involves: 129S4/SvJae * C57BL/6J * C57BL/6N J:193232 View
Fanconi anemia complementation group D2 Fancd2em1Tzh/Fancd2em1Tzh C57BL/6-Fancd2em1Tzh J:284566 View
Fanconi anemia complementation group D2 Fancd2Gt(OST57859)Lex/Fancd2Gt(OST57859)Lex
Usp1tm1.1Ada/Usp1tm1.1Ada		 involves: 129S5/SvEvBrd * C57BL/6 J:146616 View
Fanconi anemia complementation group D2 Fancd2tm1Hou/Fancd2tm1Hou 129S4/SvJae-Fancd2tm1Hou J:84892 View
Fanconi anemia complementation group D2 Fancd2tm1Hou/Fancd2tm1Hou B6.129S4-Fancd2tm1Hou J:84892 View
Fanconi anemia complementation group D2 Fancd2tm1Hou/Fancd2tm1Hou involves: 129S4/SvJae * C57BL/6J J:84892 View
Fukuyama congenital muscular dystrophy Dysfim/Dysfim
Fktntm1Ttd/Fktntm2(FCMD)Ttd		 involves: 129S7/SvEvBrd * C57BL/6 * SJL/J J:221523 View
Fukuyama congenital muscular dystrophy Fktntm1Kcam/Fktntm1Kcam
Myf5tm3(cre)Sor/Myf5+		 involves: 129S/SvEv * 129S4/SvJaeSor J:187144 View
Fukuyama congenital muscular dystrophy Fktntm1Kcam/Fktntm1Kcam
Tg(CAG-cre/Esr1*)5Amc/?		 involves: 129S/SvEv * C57BL/6 * CBA J:187144 View
Fukuyama congenital muscular dystrophy Fktntm1Kcam/Fktntm1Kcam
Tg(Ckmm-cre)5Khn/?		 involves: 129S/SvEv * FVB J:187144 View
Fukuyama congenital muscular dystrophy Fktntm1Ttd/Fktntm1Ttd involves: 129S7/SvEvBrd * C57BL/6 J:97950 View
Fukuyama congenital muscular dystrophy Fktntm1Ttd/Fktntm2(FCMD)Ttd involves: 129S7/SvEvBrd J:144746 View
hereditary spherocytosis type 1 Ank1M1Wlst/Ank1M1Wlst involves: 129S1/SvImJ * C3H/HeJ * C57BL/6 J:170562 View
hereditary spherocytosis type 1 Ank1nb/Ank1nb either: (involves: non-inbred stock) or (involves: C57BL/6) or (involves: WB/Re) J:11441 View
hereditary spherocytosis type 1 Ank1pale/Ank1pale C57BL/6J-Ank1pale/GrsrJ J:222308 View
hereditary spherocytosis type 1 Ank1Rbc2/Ank1Rbc2 involves: 129S1/Sv * BALB/c J:148127 View
hereditary spherocytosis type 3 Spta1ihj/Spta1ihj involves: HRS/J * LAH J:157766 View
hereditary spherocytosis type 3 Spta1sph-2Bc/Spta1sph-2Bc involves: SELH J:7048, J:7501 View
hereditary spherocytosis type 3 Spta1sph-ha/Spta1sph-ha involves: DBA/1J J:14946, J:30699 View
hereditary spherocytosis type 3 Spta1sph/Spta1sph either: (B6.C3-Spta1sph x WB.C3-Spta1sph)F1 or (WB.C3-Spta1sph x B6.C3-Spta1sph)F1 J:6695 View
hereditary spherocytosis type 3 Spta1sph/Spta1sph involves: C3H J:12276 View
holoprosencephaly 2 Six3tm1Gco/Six3tm1Gco involves: 129S1/Sv J:81797 View
holoprosencephaly 2 Six3tm3.1Gco/Six3+
Shhtm1Chg/Shh+		 involves: 129S1/Sv * 129X1/SvJ * C57BL/6 J:140315 View
holoprosencephaly 2 Six3tm3Gco/Six3tm3Gco
Foxg1tm1(cre)Skm/Foxg1+		 involves: 129S1/Sv * C57BL/6 J:140315 View
holoprosencephaly 2 Six3tm4(cre/ERT2)Gco/Six3+ involves: 129S1/Sv * C57BL/6 J:140315 View
holoprosencephaly 3 Disp1icb/Disp1tm1Amc
Shhtm1Amc/Shh+		 involves: 129X1/SvJ * C57BL/6J J:92058 View
holoprosencephaly 3 Shhtm1Chg/Shhtm1Chg involves: 129S1/Sv * 129X1/SvJ J:35802 View
holoprosencephaly 3 Shhtm1Chg/Shhtm1Chg involves: C57BL/6 J:89364 View
holoprosencephaly 5 Zic2Ku/Zic2Ku 129S.CAnNCrl(C3)-Zic2Ku J:238567 View
holoprosencephaly 5 Zic2Ku/Zic2Ku C3.CAnNCrl-Zic2Ku J:138862 View
holoprosencephaly 5 Zic2tm1Jaru/Zic2tm1Jaru involves: 129S4/SvJae * C57BL/6 J:60644 View
holoprosencephaly 11 Boctm1Rsk/Boc+
Cdontm1Rsk/Cdontm1Rsk		 involves: 129/Sv * 129S6/SvEvTac J:171767 View
holoprosencephaly 11 Boctm1Rsk/Boctm1Rsk
Cdontm1Rsk/Cdontm1Rsk		 B6.129-Boctm1Rsk Cdontm1Rsk J:171767 View
holoprosencephaly 11 Boctm1Rsk/Boctm1Rsk
Cdontm1Rsk/Cdontm1Rsk		 involves: 129/Sv * 129S6/SvEvTac J:171767 View
holoprosencephaly 11 Boctm2Rsk/Boc+
Cdontm1Rsk/Cdontm1Rsk		 involves: 129/Sv * 129S6/SvEvTac J:171767 View
holoprosencephaly 11 Boctm2Rsk/Boctm2Rsk
Cdontm1Rsk/Cdontm1Rsk		 B6.129-Boctm2Rsk Cdontm1Rsk J:171767 View
holoprosencephaly 11 Boctm2Rsk/Boctm2Rsk
Cdontm1Rsk/Cdontm1Rsk		 involves: 129/Sv * 129S6/SvEvTac J:171767 View
holoprosencephaly 11 Cdontm1Rsk/Cdontm1Rsk involves: 129/Sv * C57BL/6 J:82221 View
holoprosencephaly 11 Cdontm2Rsk/Cdontm2Rsk involves: 129/Sv * C57BL/6 J:82221 View
hypoplastic left heart syndrome Nkx2-5tm2.1Mwc/Nkx2-5+ B6J.Cg-Nkx2-5tm2.1Mwc/Mwc J:239808 View
hypoplastic left heart syndrome Nkx2-5tm3.1Mwc/Nkx2-5+ B6J.Cg-Nkx2-5tm3.1Mwc/Mwc J:239808 View
isolated cryptophthalmia Frem2em1Hali/Frem2em2Hali C57BL/6J-Frem2em1Hali Frem2em2Hali J:279933 View
Leber congenital amaurosis 1 Gucy2ecpfl9/Gucy2ecpfl9 B6;129P2-Gucy2ecpfl9/BocJ J:269362 View
Leber congenital amaurosis 1 Gucy2etm1Gar/Gucy2etm1Gar
Gucy2ftm1Wbae/Gucy2ftm1Wbae		 involves: 129S6/SvEvTac J:120903 View
Leber congenital amaurosis 1 Gucy2etm1Gar/Gucy2etm1Gar
Nrltm1Asw/Nrltm1Asw		 involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6 J:241970 View
Leber congenital amaurosis 2 Cnga3tm1Biel/Cnga3tm1Biel
Rpe65tm1Tmr/Rpe65tm1Tmr		 involves: 129S1/Sv * 129X1/SvJ * C57BL/6 J:71529 View
Leber congenital amaurosis 2 Rpe65rd12/Rpe65rd12 B6(A)-Rpe65rd12/J J:104929 View
Leber congenital amaurosis 2 Rpe65tm1Tmr/Rpe65tm1Tmr involves: 129S1/Sv * 129X1/SvJ J:136882 View
Leber congenital amaurosis 2 Rpe65tm1Tmr/Rpe65tm1Tmr involves: 129S1/Sv * 129X1/SvJ * C57BL/6 J:51293, J:61889, J:71529, J:81027, J:85796 View
Leber congenital amaurosis 3 Spata7tm1Mrd/Spata7tm1Mrd involves: 129S7/SvEvBrd J:216279 View
Leber congenital amaurosis 3 Spata7tm1Mrd/Spata7tm2Mrd
Tg(Crx-cre)1Tfur/0		 involves: 129S7/SvEvBrd J:279827 View
Leber congenital amaurosis 4 Aipl1tm1Mad/Aipl1tm1Mad involves: 129S7/SvEvBrd J:94655 View
Leber congenital amaurosis 4 Aipl1tm1Tili/Aipl1tm1Tili involves: 129S4/SvJae * C57BL/6 J:92601 View
Leber congenital amaurosis 4 Aipl1tm1Visu/Aipl1tm1Visu involves: 129S1/Sv * 129X1/SvJ * C57BL/6J J:92617 View
Leber congenital amaurosis 4 Aipl1tvrm119/Aipl1tvrm119 C57BL/6J-Aipl1tvrm119/Pjn J:243745 View
Leber congenital amaurosis 4 Aipl1tvrm127/Aipl1tvrm127 C57BL/6J-Aipl1tvrm127/Pjn J:243745 View
Leber congenital amaurosis 5 Lca5Gt(AG0283)Wtsi/Lca5Gt(AG0283)Wtsi involves: 129P2/OlaHsd * C57BL/6 J:174018 View
Leber congenital amaurosis 6 Rpgrip1nmf247/Rpgrip1nmf247 C57BL/6J-Rpgrip1nmf247 J:243745 View
Leber congenital amaurosis 6 Rpgrip1tm1Tili/Rpgrip1tm1Tili involves: 129S4/SvJae * C57BL/6 J:82755 View
Leber congenital amaurosis 6 Rpgrip1tvrm111/Rpgrip1tvrm111 C57BL/6J-Rpgrip1tvrm111/Pjn J:243745 View
Leber congenital amaurosis 7 Crxem2Smgc/Crx+ C57BL/6J-Crxem2Smgc J:343281 View
Leber congenital amaurosis 7 CrxRip/Crx+ C57BL/6J-CrxRip J:203337 View
Leber congenital amaurosis 7 Crxtm1Clc/Crxtm1Clc involves: 129S6/SvEvTac J:58796 View
Leber congenital amaurosis 8 Crb1rd8/Crb1rd8 STOCK Crb1rd8/J J:171736 View
Leber congenital amaurosis 8 Crb1tm1Wij/Crb1+
Crb2tm1.1Wij/Crb2tm1.1Wij
Tg(Chx10-EGFP/cre,-ALPP)2Clc/0		 involves: 129P2/OlaHsd * C57BL/6 * C57BL/6JOlaHsd * SJL J:207895 View
Leber congenital amaurosis 8 Crb1tm1Wij/Crb1tm1Wij
Crb2tm1.1Wij/Crb2tm1.1Wij
Tg(Chx10-EGFP/cre,-ALPP)2Clc/0		 involves: 129P2/OlaHsd * C57BL/6 * C57BL/6JOlaHsd * SJL J:207895 View
Leber congenital amaurosis 9 Nmnat1imh/Nmnat1imh B6J.C(C3H)-Nmnat1imh J:234111 View
Leber congenital amaurosis 9 Nmnat1tm1Ruch/Nmnat1tm1d(EUCOMM)Wtsi involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6J * C57BL/6N J:267630 View
Leber congenital amaurosis 10 Cep290rd16/Cep290rd16 involves: BXD24/TyJ J:125553 View
Leber congenital amaurosis 10 Cep290rd16/Cep290rd16 involves: BXD24/TyJ * C57BL/6 J:169232 View
Leber congenital amaurosis 10 Cep290rd16/Cep290rd16
Nrltm1Asw/Nrltm1Asw		 involves: 129S1/Sv * 129X1/SvJ * BXD24/TyJ * C57BL/6 J:169232 View
Leber congenital amaurosis 12 Rd3rd3/Rd3rd3 RBF/DnJ-Rd3rd3 J:202634 View
Leber congenital amaurosis 14 Lrattm1Kpal/Lrattm1Kpal involves: 129S6/SvEvTac J:136882 View
Leber congenital amaurosis 19 Usp45em1Qzha/Usp45em1Qzha C57BL/6J-Usp45em1Qzha J:282594 View
lissencephaly Pafah1b1tm1Awb/Pafah1b1+ involves: 129S6/SvEvTac * NIH Black Swiss J:49531, J:59817 View
lissencephaly Pafah1b1tm1Awb/Pafah1b1+
Ywhaetm1Awb/Ywhae+		 either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * NIH Black Swiss) J:84075 View
lissencephaly Pafah1b1tm1Awb/Pafah1b1tm2Awb involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss J:49531 View
lissencephaly Pafah1b1tm1Or/Pafah1b1+ Not Specified J:69631 View
lissencephaly Pafah1b1tm2.2Awb/Pafah1b1+ involves: 129S6/SvEvTac * NIH Black Swiss J:49531 View
lissencephaly Tuba1aJna/Tuba1a+ involves: BALB/cAnN * C3H/HeH J:117881 View
megaconial type congenital muscular dystrophy Chkbrmd/Chkbrmd involves: BALB/cByJ * C57BL/6J J:108320 View
microcephaly AspmGt(AA0137)Wtsi/AspmGt(AA0137)Wtsi involves: 129P2/OlaHsd * C57BL/6JOlaHsd J:164424 View
microcephaly AspmGt(AJ0069)Wtsi/AspmGt(AJ0069)Wtsi involves: 129P2/OlaHsd * C57BL/6JOlaHsd J:164424 View
microcephaly Aspmtm1(cre)Mrc/Aspmtm1(cre)Mrc Not Specified J:228026 View
microcephaly Cdk5rap2an/Cdk5rap2an B6.Cg-Cdk5rap2an J:160533 View
microcephaly Cdk5rap2an/Cdk5rap2an
Tyrp1B-lt/Tyrp1B-lt		 WBB6F1 J:160533 View
microcephaly Mcph1Gt(RRO608)Byg/Mcph1Gt(RRO608)Byg involves: 129P2/OlaHsd * C57BL/6 J:157993 View
microvillus inclusion disease Myo5btm1.1Cle/Myo5btm1.1Cle
Tg(Vil1-cre/ERT2)23Syr/0		 involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6 * DBA/2 J:227079 View
microvillus inclusion disease Myo5btm1a(KOMP)Wtsi/Myo5btm1a(KOMP)Wtsi C57BL/6N-Myo5btm1a(KOMP)Wtsi J:229427 View
muscular dystrophy-dystroglycanopathy type B1 Pomt1tm1c(EUCOMM)Hmgu/Pomt1tm1c(EUCOMM)Hmgu
Tg(Crx-cre)1Tfur/0		 involves: C57BL/6N J:263043 View
muscular dystrophy-dystroglycanopathy type B5 Fkrptm1Itl/Fkrptm1Itl involves: 129S6/SvEvTac * C57BL/6N J:164448 View
muscular dystrophy-dystroglycanopathy type B6 Large1myd-3J/Large1myd-3J STOCK Large1myd-3J/GrsrJ J:160357 View
myotonia congenita Clcn1adr-mto/Clcn1adr-mto SWR/J-Clcn1adr-mto/J J:16954 View
myotonia congenita Clcn1adr/Clcn1adr A2G-Clcn1adr J:18371 View
myotonia congenita Clcn1em1Btlr/Clcn1em1Btlr C57BL/6J-Clcn1em1Btlr J:307652 View
myotonia congenita Clcn1m1Btlr/Clcn1m1Btlr C57BL/6J-Clcn1m1Btlr J:307652 View
neonatal diabetes mellitus with congenital hypothyroidism Glis3tm1Amj/Glis3tm1Amj involves: 129 * C57BL/6 J:148994 View
neonatal diabetes mellitus with congenital hypothyroidism Glis3tm1Hiha/Glis3tm1Hiha involves: C57BL/6 * CBA J:150077 View
neural tube defect Celsr1Crsh/Celsr1+
Vangl2Lp/Vangl2+		 C3H.Cg-Vangl2Lp Celsr1Crsh J:216413 View
neural tube defect Mthfd1ltm1b(EUCOMM)Wtsi/Mthfd1ltm1b(EUCOMM)Wtsi involves: C57BL/6N * FVB/N J:193285 View
neural tube defect Mthfrtm1Rzn/Mthfrtm1Rzn involves: 129S1/Sv * 129X1/SvJ * BALB/c J:67779 View
neural tube defect ScribCrc/Scrib+
Vangl2Lp/Vangl2+		 C3H.Cg-Vangl2Lp ScribCrc J:216413 View
neural tube defect Vangl1Gt(XL802)Byg/Vangl1+
Vangl2Lp/Vangl2+		 involves: 129P2/OlaHsd * C57BL/6J * LPT/LeJ J:132697 View
neural tube defect Vangl2Lp/Vangl2Lp involves: CBA/Ca * LPT/Le J:47700 View
Oguchi disease-2 Grk1tm1Citb/Grk1tm1Citb involves: 129X1/SvJ * C57BL/6 J:54021 View
parietal foramina Alx4Lst-2J/Alx4Lst-2J C57BL/6J-Alx4Lst-2J/J J:223288 View
parietal foramina Msx2tm1Rilm/Msx2tm1Rilm either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6J) J:61509 View
patent ductus arteriosus Tfap2bem1Fenli/Tfap2bem1Fenli involves: C57BL/6 J:278067 View
periventricular nodular heterotopia FlnaDilp2/Y involves: BALB/cAnN * C3H/HeN * C57BL/6 J:112274 View
primary autosomal recessive microcephaly 2 with or without cortical malformations Wdr62tm1.1Jfch/Wdr62tm1.1Jfch involves: 129S1/SvImJ * C57BL/6N J:282438 View
pyruvate kinase deficiency of red cells Pklrchar4/Pklrchar4 involves: A/J * C57BL/6 J:86735 View
pyruvate kinase deficiency of red cells Pklrslc/Pklrslc CBA/NSlc-Pklrslc J:29199 View
rigid spine muscular dystrophy 1 Selenontm1.2Mred/Selenontm1.2Mred involves: 129S2/SvPas * C57BL/6 * C57BL/6J * SJL J:176499 View
subcortical band heterotopia Eml1tm1.2Ics/Eml1tm1.2Ics C57BL/6N-Eml1tm1.2Ics J:294769 View
subcortical band heterotopia Eml1tvrm360/Eml1tvrm360 C57BL/6J-Eml1tvrm360/Pjn J:297748 View
T-cell immunodeficiency, congenital alopecia, and nail dystrophy Foxn1nu-2J/Foxn1nu-2J B6(SJL)-Foxn1nu-2J/GrsrJ J:222308 View
T-cell immunodeficiency, congenital alopecia, and nail dystrophy Foxn1nu-Y/Foxn1nu-Y 101/HY-Foxn1nu-Y J:29022 View
T-cell immunodeficiency, congenital alopecia, and nail dystrophy Foxn1nu/Foxn1nu Not Specified J:11959 View
T-cell immunodeficiency, congenital alopecia, and nail dystrophy Foxn1tm1Tbo/Foxn1tm1Tbo involves: 129S1/Sv J:33796 View
tetralogy of Fallot Gja5tm1Paul/Gja5+ involves: 129S4/SvJae * C57BL/6 J:109301 View
tetralogy of Fallot Gja5tm1Paul/Gja5tm1Paul involves: 129S4/SvJae * C57BL/6 J:109301 View
tetralogy of Fallot Nkx2-5tm2.1Mwc/Nkx2-5+ B6J.Cg-Nkx2-5tm2.1Mwc/Mwc J:239808 View
tetralogy of Fallot Nkx2-5tm3.1Mwc/Nkx2-5+ B6J.Cg-Nkx2-5tm3.1Mwc/Mwc J:239808 View
tetralogy of Fallot Zfpm2tm1Sho/Zfpm2tm1Sho involves: 129S1/Sv J:62879, J:78688 View
Ullrich congenital muscular dystrophy Col6a1tm1Sngi/Col6a1tm1Sngi B6.Cg-Col6a1tm1Sngi J:278926 View
Ullrich congenital muscular dystrophy Col6a3tm2.1Chu/Col6a3+ B6.129(Cg)-Col6a3tm2.1Chu J:208903 View
visceral heterotaxy Acvr2btm1Enl/Acvr2btm1Enl either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6J) J:42018 View
visceral heterotaxy Cfc1b2b970Clo/Cfc1b2b970Clo C57BL/6J-Cfc1b2b970Clo J:175213 View
visceral heterotaxy Cfc1b2b2736.1Clo/Cfc1b2b2736.1Clo C57BL/6J-Cfc1b2b2736.1Clo J:175213 View
visceral heterotaxy Mmp21b2b873Clo/Mmp21b2b873Clo C57BL/6J-Mmp21b2b873Clo J:175213 View
visceral heterotaxy Mmp21b2b2458Clo/Mmp21b2b2458Clo C57BL/6J-Mmp21b2b2458Clo J:175213 View
visceral heterotaxy Zic3Bn/Zic3+ BNT/LeJ J:13124, J:14983, J:5776, J:62608, J:63168 View
visceral heterotaxy Zic3Bn/Zic3Bn BNT/LeJ J:13124, J:14983, J:5776, J:62608, J:63168 View
visceral heterotaxy Zic3tm1Bca/Y involves: 129S7/SvEvBrd J:75951 View
visceral heterotaxy Zic3tm1Bca/Y involves: 129S7/SvEvBrd * C57BL/6 J:75951 View
visceral heterotaxy Zic3tm1Bca/Zic3+ involves: 129S7/SvEvBrd * C57BL/6 J:75951 View
visceral heterotaxy Zic3tm1Bca/Zic3tm1Bca involves: 129S7/SvEvBrd * C57BL/6 J:75951 View
Walker-Warburg syndrome Pomgnt1Gt(OST179231)Lex/Pomgnt1Gt(OST179231)Lex involves: 129S5/SvEvBrd * C57BL/6J J:107697, J:196379 View
Walker-Warburg syndrome Pomgnt1tm1Stk/Pomgnt1tm1Stk involves: 129S/SvEv J:144928 View
X-linked cleft palate with or without ankyloglossia Tbx22tm1.1Sta/Tbx22tm1.1Sta involves: 129 * CD-1 J:153100 View
X-linked cleft palate with or without ankyloglossia Tbx22tm1.1Sta/Y involves: 129/Sv * CD-1 J:153100 View
      agnathia-otocephaly complex Foxh1b2b2662Clo/Foxh1b2b2662Clo C57BL/6J-Foxh1b2b2662Clo J:175213 View
agnathia-otocephaly complex Trappc10b2b2416Clo/Trappc10b2b2416Clo Trappc10b2b2416Clo J:175213 View
anencephaly Cecr2Gt(pGT1)1Hemc/Cecr2Gt(pGT1)1Hemc 129P2(C)-Cecr2Gt(pGT1)1Hemc J:96325 View
anencephaly Cecr2Gt(pGT1)1Hemc/Cecr2Gt(pGT1)1Hemc C.129P2-Cecr2Gt(pGT1)1Hemc J:96325 View
anencephaly Cecr2Gt(pGT1)1Hemc/Cecr2Gt(pGT1)1Hemc involves: 129P2/OlaHsd * BALB/c J:96325 View
anencephaly Efna5tm1Ddmo/Efna5tm1Ddmo involves: 129S1/Sv * 129X1/SvJ J:77779 View
anencephaly Lmo4tm1.1Gng/Lmo4tm1.1Gng involves: 129X1/SvJ J:96957 View
atrial heart septal defect 1 avc2/avc2 involves: C57BL/6J * FVB/N J:163196 View
atrial heart septal defect 1 Ccn1tm1Lfl/Ccn1+ involves: 129S4/SvJae * C57BL/6J J:126490 View
atrial heart septal defect 1 Ntf3tm1Par/Ntf3tm1Par involves: 129S1/Sv J:35639 View
atrial heart septal defect 1 pta/pta C57BL/6J-pta J:94456 View
atrioventricular septal defect avc3/avc3 involves: C57BL/6J * FVB/N J:163196 View
atrioventricular septal defect Bmp4tm1Blh/Bmp4tm3.1Blh
Tg(Tnnt2-cre)5Blh/0		 involves: 129S/Sv * Black Swiss * C57BL/6 * DBA/2 * ICR J:86001 View
atrioventricular septal defect Bmp4tm3.1Blh/Bmp4tm3.1Blh
Tg(Tnnt2-cre)5Blh/0		 involves: 129S6/SvEvTac * C57BL/6 * DBA/2 * ICR J:86001 View
atrioventricular septal defect Ccn1tm1Lfl/Ccn1tm1Lfl involves: 129S4/SvJae * C57BL/6J J:126490 View
atrioventricular septal defect Dnah11avc4/Dnah11avc4 involves: C57BL/6J * FVB/N J:163196 View
atrioventricular septal defect Gata4tm1.1Sad/Gata4+
Glyr1em1Dsr/Glyr1+
Tg(Tek-cre)1Ywa/0		 involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6J * SJL J:322763 View
atrioventricular septal defect Glyr1em1Dsr/Glyr1em1Dsr involves: C57BL/6J J:322763 View
atrioventricular septal defect Ift172avc1/Ift172avc1 involves: C57BL/6J * FVB/N J:163196 View
atrioventricular septal defect l11Jus16/l11Jus16 involves: C57BL/6J * FVB/N J:163196 View
atrioventricular septal defect Mks1avc6/Mks1avc6 involves: C57BL/6J * FVB/N J:163196 View
atrioventricular septal defect Nr1d2tm1Dgen/Nr1d2tm1Dgen B6;129P2-Nr1d2tm1Dgen/H J:232480 View
atrioventricular septal defect pta/pta C57BL/6J-pta J:94456 View
autosomal recessive congenital ichthyosis 4B Cst6ichq/Cst6+ involves: BALB/cJ J:41426, J:90417 View
autosomal recessive congenital ichthyosis 4B Pigatm1Tak/Pigatm1Tak
Tg(KRT5-cre)1Tak/0		 involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6 J:91794 View
autosomal recessive congenital ichthyosis 4B Pigatm1Tak/Y
Tg(KRT5-cre)1Tak/0		 involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6 J:91794 View
autosomal recessive congenital ichthyosis 4B Prss8tm1.1Hum/Prss8tm1.2Hum
Tg(KRT14-cre)1Ipc/0		 involves: 129/Sv * C57BL/6 * FVB/N * SJL J:100139 View
bladder exstrophy Trp63tm2Brd/Trp63tm2Brd involves: 129S7/SvEvBrd * C57BL/6J J:119657 View
buphthalmos Foxc1tm1Blh/Foxc1+ B6.Cg-Foxc1tm1Blh J:82280 View
buphthalmos Foxc1tm1Blh/Foxc1+
Tyrc-2J/Tyrc-2J		 B6.Cg-Tyrc-2J Foxc1tm1Blh J:82280 View
buphthalmos Tyrc-2J/Tyrc-2J B6(Cg)-Tyrc-2J/J J:82280 View
centronuclear myopathy Dnm2tm1.1Ics/Dnm2+ involves: 129S2/SvPas * C57BL/6 J:237196 View
centronuclear myopathy Klhl31em1Eno/Klhl31em1Eno involves: C57BL/6 J:247651 View
centronuclear myopathy Mtm1tm1.1Jman/Y involves: 129T1/Sv * C57BL/6 J:81791 View
cleft palate b2b1470Clo/b2b1470Clo C57BL/6J-b2b1470Clo J:175213 View
cleft palate b2b1594Clo/b2b1594Clo C57BL/6J-b2b1594Clo J:175213 View
cleft palate Cdc42tm1.1Ayam/Cdc42tm1.1Ayam
Tg(Mpz-cre)94Imeg/0		 Not Specified J:250065 View
cleft palate Golgb1em8Lanyu/Golgb1em8Lanyu FVB/NJ-Golgb1em8Lanyu J:235669 View
cleft palate Golgb1em8Lanyu/Golgb1em33Lanyu FVB/NJ-Golgb1em8Lanyu J:235669 View
cleft palate Golgb1em33Lanyu/Golgb1em33Lanyu FVB/NJ-Golgb1em8Lanyu J:235669 View
cleft palate Golgb1em33Lanyu/Golgb1m1Lanyu involves: A/J * FVB/NJ J:235669 View
cleft palate Golgb1m1Lanyu/Golgb1m1Lanyu A/J-Golgb1m1Lanyu J:235669 View
cleft palate Prmt1tm1Rchd/Prmt1tm1Rchd
H2az2Tg(Wnt1-cre)11Rth/H2az2+		 involves: 129/Sv * C57BL/6J * CBA/J J:289243 View
cleft palate Six2tm3(EGFP/cre/ERT2)Amc/Six2tm3(EGFP/cre/ERT2)Amc involves: 129/Sv * C57BL/6J J:285711 View
cleft palate Specc1lem3Kumc/Specc1l+ involves: C57BL/6J * FVB/NJ J:324294 View
cleft palate Specc1lem4Kumc/Specc1l+ involves: C57BL/6J * FVB/NJ J:324294 View
cleft soft palate Tgfbr2tm1.2Hlm/Tgfbr2tm1.2Hlm
Tg(KRT14-cre)52Smr/0		 involves: 129S6/SvEvTac * C57BL/6J * SJL/J J:208431 View
congenital amegakaryocytic thrombocytopenia Mpltm1Fjs/Mpltm1Fjs involves: 129 * C57BL/6J J:87416 View
congenital aphakia Foxe3dyl/Foxe3dyl BALB/cLiA-Foxe3dyl J:59880, J:76605 View
congenital central hypoventilation syndrome Tlx3tm1Sjk/Tlx3tm1Sjk involves: 129X1/SvJ J:60751 View
congenital chylothorax Elk3tm1Wlyk/Elk3tm1Wlyk either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6) J:71816 View
congenital chylothorax Itga9tm1Des/Itga9tm1Des involves: 129S4/SvJae * C57BL/6 J:63038 View
congenital diaphragmatic hernia b2b1528Clo/b2b1528Clo C57BL/6J-b2b1528Clo J:175213 View
congenital diaphragmatic hernia Gata4tm1.1Sad/Gata4tm1.2Sad
Tg(Prrx1-cre)1Cjt/0		 involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL/J J:231793 View
congenital diaphragmatic hernia Gata4tm1.2Wtp/Gata4+ B6.Cg-Gata4tm1.2Wtp J:117367 View
congenital diaphragmatic hernia hpld/hpld Not Specified J:75360 View
congenital diaphragmatic hernia Kif7dda/Kif7dda FVB.A-Kif7dda J:197449 View
congenital diaphragmatic hernia Lrp1b2b1554Clo/Lrp1b2b1554Clo C57BL/6J-Lrp1b2b1554Clo J:175213 View
congenital diaphragmatic hernia Ndst1tm1Je/Ndst1tm1Je
Tg(Tek-cre)1Ywa/0		 involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL J:208012 View
congenital diaphragmatic hernia Nkx3-2tm1(cre)Tsa/Nkx3-2+
Nr2f2tm2.1Tsa/Nr2f2tm2.1Tsa		 involves: 129S7/SvEvBrd * C57BL/6 J:103437 View
congenital diaphragmatic hernia Pdgfratm2Sor/Pdgfratm2Sor involves: 129S4/SvJaeSor * C57BL/6 J:160875 View
congenital diaphragmatic hernia Slit3Gt(OST106158)Lex/Slit3Gt(OST106158)Lex involves: 129S5/SvEvBrd * C57BL/6 J:86149 View
congenital diaphragmatic hernia Slit3tm1.1Dor/Slit3tm1.1Dor involves: 129S1/Sv * C57BL/6 J:208012 View
congenital diaphragmatic hernia Slit3tm1.1Dor/Slit3tm1.1Dor involves: 129S1/Sv * C57BL/6J J:83292 View
congenital diaphragmatic hernia Slit3tm1Dor/Slit3tm1Dor involves: 129S1/Sv * C57BL/6J J:83292 View
congenital diaphragmatic hernia Sox7tm1.1Dsco/Sox7+ involves: 129S/SvEv * C57BL/6 J:187416 View
congenital diaphragmatic hernia Wt1tm1.1Ndha/Wt1tm1.1Ndha
Tg(Gata4*G2-cre)#Roja/0		 involves: 129P2/OlaHsd J:238024 View
congenital diaphragmatic hernia Wt1tm1Jae/Wt1tm1Jae involves: 129S4/SvJae * C57BL/6 * MF1 J:114565 View
congenital disorder of glycosylation type I Pmm2tm1.1Jins/Pmm2tm2.1Jins involves: 129S6/SvEvTac * C57BL/6J J:23604 View
congenital dyserythropoietic anemia Diaph3tm1.1Pji/Diaph3tm1.1Pji
Tg(Mx1-cre)1Cgn/0		 involves: C57BL/6J * CBA/J J:293763 View
congenital dyserythropoietic anemia Man2a1tm1Jxm/Man2a1tm1Jxm involves: 129S1/Sv * 129X1/SvJ * C57BL/6 J:41621 View
congenital fibrosis of the extraocular muscles Kif21atm1.1Ece/Kif21a+ involves: 129S1/Sv * 129S4/SvJae J:213171 View
congenital fibrosis of the extraocular muscles Kif21atm1.1Ece/Kif21atm1.1Ece involves: 129S1/Sv * 129S4/SvJae J:213171 View
congenital fibrosis of the extraocular muscles Kif21atm1.1Ece/Kif21atm1.1Ece
Tg(Isl1-EGFP*)1Slp/0		 involves: 129S1/Sv * 129S4/SvJae * BALB/c * C57BL/6 J:213171 View
congenital fibrosis of the extraocular muscles Tubb3tm1.1Ece/Tubb3tm1.1Ece involves: 129S/SvEv * C57BL/6J J:158992 View
congenital generalized lipodystrophy type 2 Ppargtm2(tTA)Yba/Pparg+ involves: 129S1/SvImJ * C57BL/6 J:125992 View
congenital generalized lipodystrophy type 2 Ppargtm3(tTA)Yba/Pparg+ involves: 129S1/SvImJ * C57BL/6 J:125992 View
congenital heart disease b2b243.1Clo/b2b243.1Clo C57BL/6J-b2b243.1Clo J:175213 View
congenital heart disease b2b243Clo/b2b243Clo C57BL/6J-b2b243Clo J:175213 View
congenital heart disease b2b520Clo/b2b520Clo C57BL/6J-b2b520Clo J:175213 View
congenital heart disease b2b913Clo/b2b913Clo C57BL/6J-b2b913Clo J:175213 View
congenital heart disease b2b1639Clo/b2b1639Clo C57BL/6J-b2b1639Clo J:175213 View
congenital heart disease Foxj1tm1.1(cre/ERT2/GFP)Htg/Foxj1tm1.1(cre/ERT2/GFP)Htg STOCK Foxj1tm1.1(cre/ERT2/GFP)Htg/J J:342078 View
congenital heart disease Rxratm1Rev/Rxra+ involves: 129S4/SvJae * C57BL/6 J:35363 View
congenital heart disease Sap130b2b635.2Clo/Sap130b2b635.2Clo C57BL/6J-Sap130b2b635.2Clo J:242757 View
congenital heart disease Sap130b2b635.2Clo/Sap130b2b635.2Clo C57BL/6J-Sap130b2b635.2Clo Pcdha9b2b635.1Clo J:242757 View
congenital hypothyroidism Foxe1tm1Rdl/Foxe1tm1Rdl involves: 129S1/Sv * 129X1/SvJ * C57BL/6 J:48970 View
congenital hypothyroidism Runx2tm1Kish/Runx2+ involves: 129P2/OlaHsd * C57BL/6 J:162258 View
congenital hypothyroidism Slc26a7tm1Sole/Slc26a7tm1Sole involves: 129 J:325346 View
congenital hypothyroidism Tgcog/Tgcog involves: AKR/J * C57BL/6By J:8567 View
congenital hypothyroidism Trhrtm1Bau/Trhrtm1Bau involves: 129S1/Sv * 129X1/SvJ * C57BL/6 J:220755 View
congenital hypothyroidism Tshrhyt-3J/Tshrhyt-3J CByJ;CXB10-Tshrhyt-3J/GrsrJ J:210510 View
congenital hypothyroidism Tshrhyt-3J/Tshrhyt-3J CXB10/HiAJ-Tshrhyt-3J/GrsrJ J:210510 View
congenital hypothyroidism Tshrhyt/Tshrhyt CBy.RF-Tshrhyt/J J:110962, J:130062 View
congenital hypothyroidism Tshrtm1Rmar/Tshrtm1Rmar involves: 129S1/Sv * C57BL/6J J:80513 View
congenital muscular dystrophy Col6a3tm1Chu/Col6a3tm1Chu B6.129-Col6a3tm1Chu J:198581 View
congenital nervous system abnormality Eml1heco/? involves: CD-1 J:211342 View
congenital nervous system abnormality Eml1heco/Eml1heco involves: C57BL/6 * NOR J:208031 View
congenital nervous system abnormality Eml1heco/Eml1heco involves: NOR J:208031 View
congenital nervous system abnormality Tuba1aem1Rstot/Tuba1aem1Rstot involves: C57BL/6J * C57BL/6N J:278765 View
congenital nervous system abnormality Tuba1aem1Rstot/Tuba1aquas involves: C57BL/6J * C57BL/6N J:278765 View
congenital nervous system abnormality Tuba1aem2Rstot/Tuba1aem2Rstot involves: C57BL/6J * C57BL/6N J:278765 View
congenital nystagmus Ahrtm1Yfk/Ahrtm1Yfk involves: 129S/SvEv * C57BL/6J J:195817 View
dextro-looped transposition of the great arteries Cfc1tm1Cbm/Cfc1tm1Cbm Not Specified J:58530 View
dextro-looped transposition of the great arteries Dvl2tm1Awb/Dvl2tm1Awb either: 129S6/SvEvTac-Dvl2tm1Awb or (involves: 129S6/SvEvTac * NIH Swiss) J:96661 View
dextro-looped transposition of the great arteries Hspg2tm1Ref/Hspg2tm1Ref involves: 129S1/Sv * 129X1/SvJ J:80720, J:107987 View
Diamond-Blackfan anemia Flvcr1tm1.1Jlab/Flvcr1tm1.1Jlab involves: 129S4/SvJae * C57BL/6 * DBA/2 J:132057 View
Diamond-Blackfan anemia Flvcr1tm1Jlab/Flvcr1tm1Jlab
Tg(Mx1-cre)1Cgn/0		 involves: 129S4/SvJae * C57BL/6 * CBA J:132057 View
Diamond-Blackfan anemia Rpsatm1Ells/Rpsa+ involves: 129S6/SvEvTac * C57BL/6 J:138267 View
double outlet right ventricle Cfc1tm1Cbm/Cfc1tm1Cbm Not Specified J:58530 View
double outlet right ventricle Ece1tm1Reh/Ece1tm1Reh involves: 129S6/SvEvTac * C57BL/6J J:62261 View
double outlet right ventricle Ece1tm1Reh/Ece1tm1Reh
Ece2tm1Ywa/Ece2tm1Ywa		 involves: 129S6/SvEvTac * C57BL/6J J:62261 View
Fanconi anemia Usp1tm1.1Ada/Usp1tm1.1Ada C57BL/6-Usp1tm1.1Ada J:146616 View
gastroschisis Lrp1b2b1554Clo/Lrp1b2b1554Clo C57BL/6J-Lrp1b2b1554Clo J:175213 View
hereditary spherocytosis Klf1Nan/Klf1+ either: B6.Cg-Klf1Nan or WB.Cg-Klf1Nan J:162530 View
hereditary spherocytosis type 1 Add2tm1Llp/Add2tm1Llp involves: 129S4/SvJae * C57BL/6J J:71029 View
hereditary spherocytosis type 1 Epb42tm1Llp/Epb42tm1Llp involves: 129P2/OlaHsd * C57BL/6J J:67412 View
hereditary spherocytosis type 1 Spta1sph-2Bc/Spta1sph-2Bc involves: SELH J:7048, J:7501 View
hereditary spherocytosis type 1 Spta1sph-ha/Spta1sph-ha involves: DBA/1J J:14946, J:30699 View
hereditary spherocytosis type 1 Spta1sph/Spta1sph involves: C3H J:12276 View
hereditary spherocytosis type 4 Slc4a1wan/Slc4a1wan C3H/HeJ-Slc4a1wan/J J:89043 View
holoprosencephaly NosipGt(OST138992)Lex/NosipGt(OST138992)Lex B6.129S5-NosipGt(OST138992)Lex J:245546 View
holoprosencephaly Pgap1m1Nisw/Pgap1m1Nisw involves: C57BL/6J J:187360 View
holoprosencephaly Pignm1Nisw/Pignm1Nisw involves: 129S1/SvImJ * C3H/HeJ * C57BL/6J J:187360 View
hypoplastic left heart syndrome b2b464Clo/b2b464Clo C57BL/6J-b2b464Clo J:175213 View
hypoplastic left heart syndrome b2b635Clo/b2b635Clo C57BL/6J-b2b635Clo J:175213 View
hypoplastic left heart syndrome b2b1430Clo/b2b1430Clo C57BL/6J-b2b1430Clo J:175213 View
hypoplastic left heart syndrome b2b1432Clo/b2b1432Clo C57BL/6J-b2b1432Clo J:175213 View
hypoplastic left heart syndrome b2b1709Clo/b2b1709Clo C57BL/6J-b2b1709Clo J:175213 View
hypoplastic left heart syndrome b2b1963Clo/b2b1963Clo C57BL/6J-b2b1963Clo J:175213 View
hypoplastic left heart syndrome b2b3077.2Clo/b2b3077.2Clo C57BL/6J-b2b3077.2Clo J:175213 View
hypoplastic left heart syndrome b2b3077Clo/b2b3077Clo C57BL/6J-b2b3077Clo J:175213 View
hypoplastic left heart syndrome b2b3183Clo/b2b3183Clo C57BL/6J-b2b3183Clo J:175213 View
hypoplastic left heart syndrome Pcdha9em1Clo/Pcdha9em1Clo
Sap130em1Clo/Sap130em1Clo		 C57BL/6J-Sap130em1Clo Pcdha9em1Clo/MurrJ J:242757 View
hypoplastic left heart syndrome Sap130b2b635.2Clo/Sap130b2b635.2Clo C57BL/6J-Sap130b2b635.2Clo Pcdha9b2b635.1Clo J:242757 View
isolated cleft palate Satb2tm1(cre)Vit/Satb2+ involves: C57BL/6 J:116770 View
Leber congenital amaurosis Pals1tm1Caw/Pals1tm1Caw
Tg(rx3-icre)1Mjam/0		 Not Specified J:184469 View
lissencephaly Arxtm1Kki/Y involves: 129P2/OlaHsd * C57BL J:79871 View
lissencephaly Arxtm2Kki/Y involves: 129S/SvEv * C57BL/6J J:197588 View
lissencephaly Dag1tm1Kcam/Dag1tm2Kcam
Tg(GFAP-cre)25Mes/0		 involves: 129S1/Sv * 129X1/SvJ * FVB/N J:86901 View
lissencephaly Dag1tm2Kcam/Dag1tm2Kcam
Tg(GFAP-cre)25Mes/0		 involves: 129S1/Sv * 129X1/SvJ * FVB/N J:86901 View
lissencephaly Dcxtm1.2Ffr/Y either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6) J:108229 View
microcephaly Copb2em1Rstot/Copb2em2Rstot involves: C57BL/6 * C57BL/6J * CD-1 * DBA/2 J:252710 View
microcephaly Kif20bmagoo/Kif20bmagoo involves: BALB/c * C57BL/6 J:242310 View
microcephaly Ppil1em3Jgg/Ppil1em3Jgg C57BL/6-Ppil1em3Jgg J:300487 View
microcephaly Ppil1em4Jgg/Ppil1em4Jgg C57BL/6-Ppil1em4Jgg J:300487 View
microcephaly Tubb5tm1.1Dak/Tubb5tm1.1Dak
Tg(Nes-cre)1Kln/0		 involves: 129P2/OlaHsd * C57BL/6 * SJL J:240157 View
microcephaly Tubb5tm2.1Dak/Tubb5+
Tg(Nes-cre)1Kln/0		 involves: 129P2/OlaHsd * C57BL/6 * SJL J:240157 View
microvillus inclusion disease Cdc42tm1Brak/Cdc42tm1Brak
Tg(Vil1-cre)997Gum/0		 involves: C57BL/6J * SJL J:184563 View
muscular dystrophy-dystroglycanopathy type B1 B4gat1m1Ddg/B4gat1tm1(KOMP)Vlcg involves: C3H/He * C57BL/6 * C57BL/6NTac J:194150 View
muscular dystrophy-dystroglycanopathy type B1 Fkrptm1Itl/Fkrptm1Itl involves: 129S6/SvEvTac * C57BL/6N J:164448 View
muscular dystrophy-dystroglycanopathy type B1 Fkrptm1Scbr/? Not Specified J:258757 View
muscular dystrophy-dystroglycanopathy type B1 Fktntm1Ttd/Fktntm2(FCMD)Ttd involves: 129S7/SvEvBrd J:144746 View
muscular dystrophy-dystroglycanopathy type B1 Fktntm3.1Ttd/Fktntm3.1Ttd
Myf5tm3(cre)Sor/Myf5+		 involves: 129S4/SvJaeSor * C57BL/6 J:198535 View
muscular dystrophy-dystroglycanopathy type B1 Fktntm3.1Ttd/Fktntm3.1Ttd
Tg(Ckmm-cre)5Khn/0		 involves: C57BL/6 * FVB J:198535 View
muscular dystrophy-dystroglycanopathy type B1 Large1m1Btlr/Large1m1Btlr C57BL/6J-Large1m1Btlr J:307652 View
muscular dystrophy-dystroglycanopathy type B1 Large1myd/Large1myd B6.Cg-Large1myd/Pjn J:100214 View
muscular dystrophy-dystroglycanopathy type B1 Large1vls/Large1vls B6.CAST(Cg)-Large1vls/Pjn J:100214 View
muscular dystrophy-dystroglycanopathy type B1 Pomgnt1tm1.1Cfg/Pomgnt1tm1.1Cfg involves: C57BL/6 J:258757 View
neural tube defect Lrp6Cd/Lrp6Cd A-Lrp6Cd J:58433, J:101423 View
neural tube defect Pax3Sp-1Wli/Pax3Sp-1Wli involves: C57BL/6J * CBA/CaJ J:196572 View
neurogenic-type arthrogryposis multiplex congenita-2 pma/pma involves: CF-1 J:8195 View
omphalocele Lrp1b2b1554Clo/Lrp1b2b1554Clo C57BL/6J-Lrp1b2b1554Clo J:175213 View
orofacial cleft Msx1tm1Rilm/Msx1tm1Rilm either: (involves: 129S4/SvJae-Msx1tm1Rilm) or (involves: 129S4/SvJae * BALB/c) or (involves: 129X1/SvJae * C57BL/6J) J:17489 View
orofacial cleft Tfap2atm1Will/Tfap2atm2.1Will involves: 129S1/Sv * Black Swiss J:217408 View
patent ductus arteriosus Myocdtm1Msp/Myocdtm1Msp
H2az2Tg(Wnt1-cre)11Rth/H2az2+		 involves: 129/Sv * C57BL/6 * CBA J:131288 View
patent ductus arteriosus Myocdtm1Msp/Myocdtm1Msp
Tg(Pax3-cre)1Joe/0		 involves: 129/Sv * C57BL/6 * SJL J:131288 View
physical disorder Bmp4tm4Blh/Bmp4tm4Blh
Isl1tm1(cre)Sev/Isl1+		 involves: 129 * 129S6/SvEvTac J:192045 View
polydactyly Cibar1tm1b(KOMP)Wtsi/Cibar1tm1b(KOMP)Wtsi C57BL/6N-Cibar1tm1b(KOMP)Wtsi/Wtsi J:274784 View
right atrial isomerism Acvr2btm1Enl/Acvr2btm1Enl either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6J) J:42018 View
right atrial isomerism Cfc1tm1Cbm/Cfc1tm1Cbm Not Specified J:58530 View
right atrial isomerism Cfc1tm1Mms/Cfc1tm1Mms either: (involves: 129S6/SvEvTac * Black Swiss) or (involves: 129S6/SvEvTac * C57BL/6J) J:58104 View
scimitar syndrome Ift88tm1Bky/Ift88tm1Rpw
Tg(Col1a1-cre)1Bek/0		 involves: 129 * 129P2/OlaHsd * CD-1 J:308860 View
scimitar syndrome Pdgfratm2Sor/Pdgfratm2Sor involves: 129S4/SvJaeSor J:157946 View
severe congenital neutropenia Gfi1Gen/Gfi1+ C57BL/6J-Gfi1Gen J:182679 View
spina bifida Fkbp8Gt(OST287985)Lex/Fkbp8Gt(OST287985)Lex involves: 129S5/SvEvBrd * C57BL/6 J:132031 View
tetralogy of Fallot Bmp10b2b2711Clo/Bmp10b2b2711Clo C57BL/6J-Bmp10b2b2711Clo J:175213 View
tetralogy of Fallot Cited2tm1Ycy/Cited2tm1Ycy involves: C57BL/6J J:78364 View
tetralogy of Fallot Del(11Mpo-Chad)18Brd/+ involves: 129S7/SvEvBrd * C57BL/6 J:109163 View
tetralogy of Fallot Dnah5hlb612/Dnah5hlb612 involves: C57BL/6J J:130755 View
tetralogy of Fallot Dock1b2b3190Clo/Dock1b2b3190Clo C57BL/6J-Dock1b2b3190Clo J:175213 View
tetralogy of Fallot Fgf8tm1.3Mrt/Fgf8tm1.4Mrt
Tg(Msx2-cre)5Rem/0		 involves: 129P2/OlaHsd J:66266 View
tetralogy of Fallot Hey2tm1Uts/Hey2tm1Uts either: (involves: 129X1/SvJ) or (involves: C57BL/6) J:79025 View
tetralogy of Fallot Invsinv/Invsinv FVB/N-Invsinv J:48533 View
tetralogy of Fallot Mks1avc6/Mks1avc6 involves: C57BL/6J * FVB/N J:163196 View
tetralogy of Fallot Ntf3tm1Par/Ntf3tm1Par involves: 129S1/Sv J:35639 View
tetralogy of Fallot Phc1tm1Os/Phc1tm1Os involves: 129S2/SvPas * C57BL/6 J:43764 View
visceral heterotaxy 1700093K21Rikb2b3025Clo/1700093K21Rikb2b3025Clo C57BL/6J-1700093K21Rikb2b3025Clo J:175213 View
visceral heterotaxy Anks6b2b1801.1Clo/Anks6b2b1801.1Clo C57BL/6J-Anks6b2b1801.1Clo J:175213 View
visceral heterotaxy Ap1b1b2b1660Clo/Ap1b1b2b1660Clo C57BL/6J-Ap1b1b2b1660Clo J:175213 View
visceral heterotaxy b2b227Clo/b2b227Clo C57BL/6J-b2b227Clo J:175213 View
visceral heterotaxy b2b386.1Clo/b2b386.1Clo C57BL/6J-b2b386.1Clo J:175213 View
visceral heterotaxy b2b386Clo/b2b386Clo C57BL/6J-b2b386Clo J:175213 View
visceral heterotaxy b2b942Clo/b2b942Clo C57BL/6J-b2b942Clo J:175213 View
visceral heterotaxy b2b997Clo/b2b997Clo C57BL/6J-b2b997Clo J:175213 View
visceral heterotaxy b2b1146Clo/b2b1146Clo C57BL/6J-b2b1146Clo J:175213 View
visceral heterotaxy b2b1163Clo/b2b1163Clo C57BL/6J-b2b1163Clo J:175213 View
visceral heterotaxy b2b1200Clo/b2b1200Clo C57BL/6J-b2b1200Clo J:175213 View
visceral heterotaxy b2b1291Clo/b2b1291Clo C57BL/6J-b2b1291Clo J:175213 View
visceral heterotaxy b2b1436Clo/b2b1436Clo C57BL/6J-b2b1436Clo J:175213 View
visceral heterotaxy b2b1456Clo/b2b1456Clo C57BL/6J-b2b1456Clo J:175213 View
visceral heterotaxy b2b1519Clo/b2b1519Clo C57BL/6J-b2b1519Clo J:175213 View
visceral heterotaxy b2b1700Clo/b2b1700Clo C57BL/6J-b2b1700Clo J:175213 View
visceral heterotaxy b2b1801Clo/b2b1801Clo C57BL/6J-b2b1801Clo J:175213 View
visceral heterotaxy b2b2025Clo/b2b2025Clo C57BL/6J-b2b2025Clo J:175213 View
visceral heterotaxy b2b2140Clo/b2b2140Clo C57BL/6J-b2b2140Clo J:175213 View
visceral heterotaxy b2b2350Clo/b2b2350Clo C57BL/6J-b2b2350Clo J:175213 View
visceral heterotaxy b2b2696.1Clo/b2b2696.1Clo C57BL/6J-b2b2696.1Clo J:175213 View
visceral heterotaxy b2b2696Clo/b2b2696Clo C57BL/6J-b2b2696Clo J:175213 View
visceral heterotaxy b2b2736Clo/b2b2736Clo C57BL/6J-b2b2736Clo J:175213 View
visceral heterotaxy Bicc1b2b222Clo/Bicc1b2b222Clo C57BL/6J-Bicc1b2b222Clo J:175213 View
visceral heterotaxy Cc2d2ab2b1035Clo/Cc2d2ab2b1035Clo C57BL/6J-Cc2d2ab2b1035Clo J:175213 View
visceral heterotaxy Ccdc39b2b1304Clo/Ccdc39b2b1304Clo C57BL/6J-Ccdc39b2b1304Clo J:175213 View
visceral heterotaxy Ccdc39b2b1735Clo/Ccdc39b2b1735Clo C57BL/6J-Ccdc39b2b1735Clo J:175213 View
visceral heterotaxy Ccdc39b2b2025.1Clo/Ccdc39b2b2025.1Clo C57BL/6J-Ccdc39b2b2025.1Clo J:175213 View
visceral heterotaxy Cep290b2b1454Clo/Cep290b2b1454Clo C57BL/6J-Cep290b2b1454Clo J:175213 View
visceral heterotaxy Cep290b2b1752Clo/Cep290b2b1752Clo C57BL/6J-Cep290b2b1752Clo J:175213 View
visceral heterotaxy Cplane2b2b2827Clo/Cplane2b2b2827Clo C57BL/6J-Cplane2b2b2827Clo J:175213 View
visceral heterotaxy Daw1b2b1116Clo/Daw1b2b1116Clo C57BL/6J-Daw1b2b1116Clo J:175213 View
visceral heterotaxy Daw1b2b1584Clo/Daw1b2b1584Clo C57BL/6J-Daw1b2b1584Clo J:175213 View
visceral heterotaxy Dnaaf3b2b1739Clo/Dnaaf3b2b1739Clo C57BL/6J-Dnaaf3b2b1739Clo J:175213 View
visceral heterotaxy Dnah5b2b002Clo/Dnah5b2b002Clo C57BL/6J-Dnah5b2b002Clo J:175213 View
visceral heterotaxy Dnah5b2b016Clo/Dnah5b2b016Clo C57BL/6J-Dnah5b2b016Clo J:175213 View
visceral heterotaxy Dnah5b2b601Clo/Dnah5b2b601Clo C57BL/6J-Dnah5b2b601Clo J:175213 View
visceral heterotaxy Dnah5b2b1003Clo/Dnah5b2b1003Clo C57BL/6J-Dnah5b2b1003Clo J:175213 View
visceral heterotaxy Dnah5b2b1134Clo/Dnah5b2b1134Clo C57BL/6J-Dnah5b2b1134Clo J:175213 View
visceral heterotaxy Dnah5b2b1537Clo/Dnah5b2b1537Clo C57BL/6J-Dnah5b2b1537Clo J:175213 View
visceral heterotaxy Dnah5b2b2395Clo/Dnah5b2b2395Clo C57BL/6J-Dnah5b2b2395Clo J:175213 View
visceral heterotaxy Dnah5b2b2451Clo/Dnah5b2b2451Clo C57BL/6J-Dnah5b2b2451Clo J:175213 View
visceral heterotaxy Dnah5b2b2925Clo/Dnah5b2b2925Clo C57BL/6J-Dnah5b2b2925Clo J:175213 View
visceral heterotaxy Dnah11b2b598Clo/Dnah11b2b598Clo C57BL/6J-Dnah11b2b598Clo J:175213 View
visceral heterotaxy Dnah11b2b1203Clo/Dnah11b2b1203Clo C57BL/6J-Dnah11b2b1203Clo J:175213 View
visceral heterotaxy Dnah11b2b1279Clo/Dnah11b2b1279Clo C57BL/6J-Dnah11b2b1279Clo J:175213 View
visceral heterotaxy Dnah11b2b1289Clo/Dnah11b2b1289Clo C57BL/6J-Dnah11b2b1289Clo J:175213 View
visceral heterotaxy Dnah11b2b1727Clo/Dnah11b2b1727Clo C57BL/6J-Dnah11b2b1727Clo J:175213 View
visceral heterotaxy Dnah11b2b1775Clo/Dnah11b2b1775Clo C57BL/6J-Dnah11b2b1775Clo J:175213 View
visceral heterotaxy Dnah11b2b2349Clo/Dnah11b2b2349Clo C57BL/6J-Dnah11b2b2349Clo J:175213 View
visceral heterotaxy Dnai1b2b1526Clo/Dnai1b2b1526Clo C57BL/6J-Dnai1b2b1526Clo J:175213 View
visceral heterotaxy Drc1b2b1654Clo/Drc1b2b1654Clo C57BL/6J-Drc1b2b1654Clo J:175213 View
visceral heterotaxy Foxh1b2b2662Clo/Foxh1b2b2662Clo C57BL/6J-Foxh1b2b2662Clo J:175213 View
visceral heterotaxy Gm572b2b1167Clo/Gm572b2b1167Clo C57BL/6J-Gm572b2b1167Clo J:175213 View
visceral heterotaxy Ift74b2b796Clo/Ift74b2b796Clo C57BL/6J-Ift74b2b796Clo J:175213 View
visceral heterotaxy Megf8b2b288Clo/Megf8b2b288Clo C57BL/6J-Megf8b2b288Clo J:175213 View
visceral heterotaxy Megf8hlb611/Megf8hlb611 involves: C57BL/6J * C3H/HeJ J:146957 View
visceral heterotaxy Odad2b2b227.1Clo/Odad2b2b227.1Clo C57BL/6J-Odad2b2b227.1Clo J:175213 View
visceral heterotaxy Odad2b2b643Clo/Odad2b2b643Clo C57BL/6J-Odad2b2b643Clo J:175213 View
visceral heterotaxy Pcsk5b2b1549Clo/Pcsk5b2b1549Clo C57BL/6J-Pcsk5b2b1549Clo J:175213 View
visceral heterotaxy Psme4b2b1508Clo/Psme4b2b1508Clo C57BL/6J-Psme4b2b1508Clo J:175213 View
visceral heterotaxy Rfx3b2b1213Clo/Rfx3b2b1213Clo C57BL/6J-Rfx3b2b1213Clo J:175213 View
visceral heterotaxy Slit2b2b1200.1Clo/Slit2b2b1200.1Clo C57BL/6J-Slit2b2b1200.1Clo J:175213 View
visceral heterotaxy Tbc1d32b2b2284Clo/Tbc1d32b2b2284Clo C57BL/6J-Tbc1d32b2b2284Clo J:175213 View
visceral heterotaxy Tmem67b2b1163.1Clo/Tmem67b2b1163.1Clo C57BL/6J-Tmem67b2b1163.1Clo J:175213 View
visceral heterotaxy Tmem67b2b1291.1Clo/Tmem67b2b1291.1Clo C57BL/6J-Tmem67b2b1291.1Clo J:175213 View
Walker-Warburg syndrome Col4a1deltaex40/Col4a1+ involves: 129S/SvEv * C57BL/6J J:172720 View
      congenital myasthenic syndrome 3A Tg(Ckm-Chrnd*S262T)40Cgz/0 involves: C57BL/6 * DBA/2 J:31221 View
congenital myasthenic syndrome 4A Chrnetm2Vwi/Chrnetm2Vwi involves: 129P2/OlaHsd * C57BL/6 J:182046 View
congenital myasthenic syndrome 4A Tg(Ckm-Chrne*L269F)5Cgz/? involves: FVB/NJ J:193524 View
congenital secretory sodium diarrhea 3 Prss8em1Bug/Prss8em1Bug
Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg		 involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * FVB/NJ * NIH Black Swiss J:261068 View
congenital stationary night blindness autosomal dominant 1 Tg(Rho*G90D*A337V)202Sie/0 involves: C57BL/6 * DBA J:188632 View
congenital stromal corneal dystrophy Tg(CAG-cat,-Dcn*)#Debi/0
Tg(Kera-cre)KC4.3Wwk/0		 involves: FVB/N J:177392 View
Diamond-Blackfan anemia Col1a1tm1(tetO-RNAi:Rps19)Karl/Col1a1+
Gt(ROSA)26Sortm1(rtTA*M2)Jae/Gt(ROSA)26Sortm1(rtTA*M2)Jae		 involves: 129S4/SvJae * C57BL/6 J:179085 View
Diamond-Blackfan anemia Col1a1tm1(tetO-RNAi:Rps19)Karl/Col1a1tm1(tetO-RNAi:Rps19)Karl
Gt(ROSA)26Sortm1(rtTA*M2)Jae/Gt(ROSA)26Sortm1(rtTA*M2)Jae		 involves: 129S4/SvJae * C57BL/6 J:179085 View
Diamond-Blackfan anemia Col1a1tm2(tetO-RNAi:Rps19)Karl/Col1a1+
Gt(ROSA)26Sortm1(rtTA*M2)Jae/Gt(ROSA)26Sortm1(rtTA*M2)Jae		 involves: 129S4/SvJae * C57BL/6 J:179085 View
Diamond-Blackfan anemia Col1a1tm2(tetO-RNAi:Rps19)Karl/Col1a1tm2(tetO-RNAi:Rps19)Karl
Gt(ROSA)26Sortm1(rtTA*M2)Jae/Gt(ROSA)26Sortm1(rtTA*M2)Jae		 involves: 129S4/SvJae * C57BL/6 J:179085 View
tetralogy of Fallot Dp(16Lipi-Zbtb21)1Yey/0 involves: 129S7/SvEvBrd J:121790 View
Transgenes and
Other Mutations		     centronuclear myopathy Tg(Myh7-Pln)2Egk/0 FVB/N-Tg(Myh7-Pln)2Egk J:224766 View
cleft palate Tg(CAG-LacZ,-ACVR1*,-EGFP)35-1Mis/0
Tg(KRT14-cre)1Amc/0		 involves: C57BL/6 * CBA * DBA/2 J:233662 View
cleft palate-lateral synechia syndrome H2az2Tg(Wnt1-cre)11Rth/H2az2+
Tg(CAG-Bmp4,-EGFP)1Ypc/0		 involves: C57BL/6J * CBA/J * CD-1 J:214763 View
congenital generalized lipodystrophy type 2 Tg(aP2-SREBF1c)9884Reh/0 involves: C57BL/6J * SJL J:50770 View
dextro-looped transposition of the great arteries Del(11Mpo-Chad)18Brd/+ involves: 129S7/SvEvBrd * C57BL/6 J:109163 View
Diamond-Blackfan anemia Tg(CAG-RPS19*R62W)#Dmb/0
Tg(Prnp-GFP/cre)1Blw/0		 involves: 129S6/SvEvTac * FVB/N J:165876 View
lethal congenital glycogen storage disease of heart Tg(Myh6-PRKAG2*T400N)1Feah/0 involves: FVB/N J:162180 View
lethal congenital glycogen storage disease of heart Tg(Myh6-tTA)55Rbns/0
Tg(Myh6/tetO-PRKAG2*N488I)1Chib/0		 Not Specified J:145090 View
Silver-Russell syndrome Tg(BAC144D14)5A2Masu/0 B6J.Cg-Tg(BAC144D14)5A2Masu J:232408 View
Silver-Russell syndrome Tg(BAC144D14)5D3Masu/0 B6.Cg-Tg(BAC144D14)5D3Masu J:239325 View
Silver-Russell syndrome Tg(BAC144D14)5D3Masu/0 B6J.Cg-Tg(BAC144D14)5D3Masu J:232408 View
Additional
Complex
Models		     atrial heart septal defect 1 Nkx2-5tm4Rph/Nkx2-5+
Tbx20tm1.1Rph/Tbx20+		 involves: 129S1/Sv * C57BL/6 J:98489 View
holoprosencephaly Chrdtm1Emdr/Chrdtm1Emdr
Nodaltm1Rob/Nodal+		 involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ J:161524 View
holoprosencephaly Nogtm1Amc/Nogtm1Amc
Smad3tm1Xfw/Smad3+		 involves: 129/Sv * 129S1/Sv J:161524 View
neural tube defect Celsr1Crsh/Celsr1+
ScribCrc/Scrib+		 C3H.Cg-ScribCrc Celsr1Crsh J:216413 View
neural tube defect Celsr1Scy/Celsr1+
ScribCrc/Scrib+		 C3H.Cg-ScribCrc Celsr1Scy J:216413 View
neural tube defect Pax1un/Pax1+
Tcf3tm1Cmu/Tcf3tm1Cmu		 involves: 129P2/OlaHsd * C3H * C57BL/6 J:103567 View

       
No similarity to the expected human disease phenotype was found.
        Disease Term Allelic Composition Genetic Background Reference Phenotypes
NOT Models      anencephaly Cecr2Gt(pGT1)1Hemc/Cecr2Gt(pGT1)1Hemc FVB.129P2(C)-Cecr2Gt(pGT1)1Hemc J:96325 View
congenital disorder of glycosylation type I MpiGt(OST90588)Lex/MpiGt(OST90588)Lex involves: 129S5/SvEvBrd * C57BL/6 J:109220 View
congenital dyserythropoietic anemia type III Kif23tm1.1Igo/Kif23+ involves: C57BL/6 * C57BL/6NTac J:321429 View
congenital dyserythropoietic anemia type III Kif23tm1.1Igo/Kif23tm1.1Igo involves: C57BL/6 * C57BL/6NTac J:321429 View
Fanconi anemia complementation group P Slx4tm1.2Jrou/Slx4tm1.2Jrou B6.129P2-Slx4tm1.2Jrou J:204996 View
holoprosencephaly 4 Tgif1tm1.1Caw/Tgif1tm1.1Caw involves: C57BL/6 * FVB/N J:97642 View
hypoplastic left heart syndrome Hand1tm5Abfi/Hand1+
Nkx2-5tm1(cre)Rjs/Nkx2-5+		 involves: 129S7/SvEvBrd J:311466 View
hypoplastic left heart syndrome Hand1tm5Abfi/Hand1+
Tg(Mef2c-cre)2Blk/0		 Not Specified J:311466 View
hypoplastic left heart syndrome Hand1tm5Abfi/Hand1+
Tg(Myh6-cre)2182Mds/0		 involves: FVB/N J:311466 View
Leber congenital amaurosis 9 Nmnat1tm1Ruch/Nmnat1tm1Ruch involves: 129S7/SvEvBrd J:267630 View
neural tube defect Vangl1Gt(XL802)Byg/Vangl1Gt(XL802)Byg involves: 129P2/OlaHsd * C57BL/6J J:132697 View
Silver-Russell syndrome Grb10Gt(Betageo)1Ward/Grb10+ involves: C57BL/6 * CBA J:84425 View
Silver-Russell syndrome Grb10Gt(Betageo)1Ward/Grb10Gt(Betageo)1Ward involves: C57BL/6 * CBA J:84425 View