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Mammalian Phenotype Ontology Annotations
Query Results - Summary
143 genotypes with 163 annotations displayed of selected term and subterms
Searched Term: abnormal digestive system development
Allelic Composition
(Genetic Background)		 Annotated Term Reference
Apctm2.1Cip/Apctm2.1Cip
Tg(Vil1-cre/ERT2)23Syr/0
(involves: 129P2/OlaHsd * C57BL/6 * DBA/2) 		abnormal intestine development J:98469
Apctm2Rak/Apctm2Rak
Tg(Pdx1-cre)6Tuv/0
(involves: 129/Sv * C57BL/6J * FVB/N * SJL) 		abnormal intestine development J:234310
Apctm3Mmt/Apctm3Mmt
(involves: 129X1/SvJ * C57BL/6N) 		abnormal foregut morphology J:81402
Bmp4tm2Blh/Bmp4tm2Blh
(involves: 129S6/SvEvTac * Black Swiss) 		abnormal foregut morphology J:71204
Bptfem1Zfa/Bptfem1Zfa
Ehfem1Zfa/Ehfem1Zfa
Lgr5tm1(cre/ERT2)Cle/Lgr5+
(involves: 129P2/OlaHsd * C57BL/6) 		abnormal digestive system development J:268724
Bptfem1Zfa/Bptfem1Zfa
Lgr5tm1(cre/ERT2)Cle/Lgr5+
(involves: 129P2/OlaHsd * C57BL/6) 		abnormal digestive system development J:268724
Cdc25atm1Hpw/Cdc25atm1.1Hpw
Cdc25btm1Pjd/Cdc25btm1Pjd
Cdc25ctm1Hpw/Cdc25ctm1Hpw
Tg(Vil1-cre/ERT2)23Syr/0
(involves: 129X1/SvJ * C57BL/6 * DBA/2) 		abnormal enterocyte differentiation J:169457
Cdc25atm1Hpw/Cdc25atm1.1Hpw
Cdc25btm1Pjd/Cdc25btm1Pjd
Tg(Vil1-cre/ERT2)23Syr/0
(involves: 129X1/SvJ * C57BL/6 * DBA/2) 		abnormal enterocyte differentiation J:169457
Cdkn1ctm1Bbd/Cdkn1ctm1Bbd
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6) 		abnormal digestive system development J:40142
Cdx2tm1Khk/Cdx2tm1Khk
Tg(Foxa3-cre)1Khk/0
(involves: C57BL/6 * DBA * SJL) 		abnormal digestive system development J:149479
abnormal hindgut morphology J:149479
Col1a1tm1(tetO-CTNNB1)Tcd/Col1a1+
Gt(ROSA)26Sortm1(rtTA*M2)Jae/Gt(ROSA)26Sor+
(involves: 129S4/SvJae * C57BL/6 * C57BL/6J) 		abnormal intestine development J:193365
Col1a1tm1(tetO-Tcfap2c)Hsc/Col1a1+
Gt(ROSA)26Sortm1(rtTA*M2)Jae/Gt(ROSA)26Sor+
(involves: 129S4/SvJae * C57BL/6) 		abnormal intestine development J:174049
Col19a1tm1Rmz/Col19a1tm1Rmz
(involves: 129S1/Sv * 129T2/SvEmsJ * 129X1/SvJ) 		abnormal esophagus development J:92510
Cplane1b2b012Clo/Cplane1b2b012Clo
(C57BL/6J-Cplane1b2b012Clo) 		abnormal intestine development J:223340
Crb2tm1Vlcg/Crb2tm1Vlcg
(B6.Cg-Crb2tm1Vlcg) 		abnormal digestive system development J:177837
abnormal foregut morphology J:177837
Csnk1a1tm1.1Ybn/Csnk1a1tm1.1Ybn
Trp53tm1Brn/Trp53tm1Brn
Tg(Vil1-cre/ERT2)23Syr/0
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2) 		abnormal intestine development J:291671
Ctnnb1tm2Kem/Ctnnb1tm2.1Kem
Gt(ROSA)26Sortm1(Ctnnb1)Kem/Gt(ROSA)26Sortm1(Ctnnb1)Kem
Tg(Cdx1-cre)23Kem/0
(involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6 * FVB) 		persistent cloaca J:187739
cy/cy
(P-cy) 		abnormal digestive system development J:6274
abnormal tailgut morphology J:6274
Cyp26a1tm1.1Hmd/Cyp26a1tm1.1Hmd
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6Cr) 		abnormal digestive system development J:67375
Cyp26a1tm1.1Ptk/Cyp26a1tm1.1Ptk
(involves: 129S2/SvPas * C57BL/6 * SJL) 		abnormal digestive system development J:67399
abnormal hindgut morphology J:67399
Dact1tm1.1Bnrc/Dact1tm1.1Bnrc
(B6.Cg-Dact1tm1.1Bnrc) 		abnormal tailgut morphology J:152701
Dact1tm1Yegc/Dact1tm1Yegc
(B6.129-Dact1tm1Yegc) 		abnormal hindgut morphology J:161177
Dnah5b2b2451Clo/Dnah5b2b2451Clo
(C57BL/6J-Dnah5b2b2451Clo) 		abnormal midgut morphology J:175213
Drd1tm1Jcd/Drd1tm1Jcd
Drd2tm1Ebo/Drd2tm1Ebo
(involves: 129S2/SvPas * 129S4/SvJae * C57BL/6) 		abnormal digestive system development J:91781
Ednrbs-l/Ednrbs-l
(involves: C3H/HeJ * C57BL/6) 		abnormal hindgut morphology J:5407
Efnb2tm1Henk/Efnb2tm1Henk
(either: 129 or (involves: 129 * C57BL/6) or (involves: 129 * CD-1)) 		persistent cloaca J:91491
Ehfem1Zfa/Ehfem1Zfa
(C57BL/6-Ehfem1Zfa) 		abnormal digestive system development J:268724
Epb41l5tm1Sia/Epb41l5tm1Sia
(Not Specified) 		abnormal foregut morphology J:142596
Ercc5tm1Shm/Ercc5tm1Shm
(involves: 129S2/SvPas * C57BL/6J) 		delayed intestine development J:53756
Etl4Gt(6LSN)6029Gos/Etl4Gt(6LSN)6029Gos
Etn2Sd/Etn2+
(involves: 129/Sv * 129S2/SvPas * C57BL/6 * NMRI) 		persistent cloaca J:49126
Etn2Sd/Etn2Sd
(Not Specified) 		persistent cloaca J:30757
Etn2Sd/Etn2Sd
(involves: Danforth's duplication stock) 		persistent cloaca J:13055
Fam20bGt(GST_4283_D8)Lex/Fam20bGt(GST_4283_D8)Lex
(involves: 129S5/SvEvBrd * C57BL/6) 		abnormal digestive system development J:186384
Fgf10tm1Ska/Fgf10tm1Ska
(involves: C57BL/6 * CBA) 		abnormal hindgut morphology J:115048
Foxa2tm1Jrt/Foxa2tm1Jrt
(involves: 129S1/Sv * 129X1/SvJ * CD-1) 		abnormal foregut morphology J:19895
Foxf1tm1Pca/Foxf1tm1Pca
(either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * CD-1) or (involves: 129X1/SvJ * C57BL/6)) 		abnormal hindgut morphology J:66591
absent midgut J:66591
Foxl1tm1Khk/Foxl1tm1Khk
(involves: 129P2/OlaHsd * C57BL/6) 		delayed intestine development J:41235
Foxp1tm1Eem/Foxp1+
Foxp2tm1Bux/Foxp2tm1Bux
(involves: 129X1/SvJ * C57BL/6) 		abnormal esophagus development J:121421
Foxp4tm1Eem/Foxp4tm1Eem
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6) 		abnormal digestive system development J:92817
Furintm1Ajmr/Furintm1Ajmr
(involves: 129P2/OlaHsd * C57BL/6) 		absent midgut J:50582
Gadd45gip1tm2Kong/Gadd45gip1tm2Kong
Tg(Vil1-cre)997Gum/0
(involves: 129P2/OlaHsd * C57BL/6J * SJL) 		abnormal digestive system development J:156319
Gata4tm1Eno/Gata4tm1Eno
(involves: 129S7/SvEvBrd * C57BL/6) 		absent foregut J:40145
Gata4tm1Jml/Gata4tm1Jml
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1) 		abnormal foregut morphology J:40144
Gata6osem1Zfa/Gata6osem1Zfa
Lgr5tm1(cre/ERT2)Cle/Lgr5+
(involves: 129P2/OlaHsd * C57BL/6) 		abnormal digestive system development J:268724
Gata6osem2Zfa/Gata6osem2Zfa
(C57BL/6-1010001N08Rikem2Zfa) 		abnormal digestive system development J:268724
Gata6osem4Zfa/Gata6osem4Zfa
(C57BL/6-1010001N08Rikem4Zfa) 		abnormal digestive system development J:268724
Gdf1tm1Sjl/Gdf1tm1Sjl
Nodaltm1Rob/Nodal+
(involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6) 		abnormal foregut morphology J:108723
Gdf11tm1Sjl/Gdf11tm1Sjl
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6) 		abnormal tailgut morphology J:272567
Gli2tm1Alj/Gli2tm1Alj
(involves: 129S1/Sv * 129X1/SvJ * CD-1) 		abnormal esophagus development J:49603
abnormal foregut morphology J:49603
Gli2tm1Alj/Gli2tm1Alj
Gli3Xt/Gli3Xt
(involves: 129S1/Sv * 129X1/SvJ * CD-1) 		abnormal esophagus development J:49603
abnormal foregut morphology J:49603
gpg3/gpg3
(involves: BALB/cAnN * C3H/HeH) 		abnormal digestive system development J:145068
Gt(ROSA)26Sortm1(Smo/EYFP)Amc/Gt(ROSA)26Sor+
Nkx3-2tm1(cre)Wez/Nkx3-2+
(involves: 129S7/SvEvBrd * 129X1/SvJ) 		abnormal intestine development J:199664
Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sortm1Sor
Ptf1atm1.1(cre)Cvw/Ptf1atm1.1(cre)Cvw
(involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * Black Swiss) 		abnormal digestive system development J:78710
Gt(ROSA)26Sortm2(tTA,CMV*1-KIAA1549/BRAF,-EGFP)Gtm/Gt(ROSA)26Sor+
Tg(Fabp7-cre,-lacZ)3Gtm/0
(involves: 129S6/SvEvTac * C57BL/6 * CBA) 		abnormal hindgut morphology J:204469
Gt(ROSA)26Sortm14(CAG-tdTomato)Hze/Gt(ROSA)26Sor+
Rr271em1Mgn/Rr271+
Sox17tm2(EGFP/cre)Mgn/Sox17+
(involves: 129S6/SvEvTac * C57BL/6NCrl * CD-1) 		truncated foregut J:328045
Hgstm1Sor/Hgstm1Sor
(either: 129/Sv-Hgstm1Sor or B6.129-Hgstm1Sor or (involves: 129/Sv * 129S4/SvJae * C57BL/6J)) 		absent foregut J:55580
Igf2bp1Gt(OST33739)Lex/Igf2bp1Gt(OST33739)Lex
(involves: 129S5/SvEvBrd * C57BL/6) 		delayed intestine development J:89882
Irf6tm1Mjd/Irf6+
SfnEr/Sfn+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6) 		abnormal esophagus development J:116077
Irf6tm1Mjd/Irf6tm1Mjd
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6) 		abnormal esophagus development J:116077
Ldb1tm1Lmgd/Ldb1tm1Lmgd
(involves: CD-1) 		abnormal foregut morphology J:81152
lec/lec
(Not Specified) 		abnormal esophagus development J:6726
abnormal foregut morphology J:6726
Lgr4tm1.1(cre/ERT2)Npa/Lgr4tm1.1(cre/ERT2)Npa
(involves: C57BL/6) 		abnormal intestine development J:212415
Lgr4tm1.1(cre/ERT2)Npa/Lgr4tm1.1(cre/ERT2)Npa
Lgr5tm1.1(cre/ERT2)Npa/Lgr5tm1.1(cre/ERT2)Npa
(involves: C57BL/6) 		abnormal intestine development J:212415
Mapk7tm1Jsca/Mapk7tm1Jsca
(either: (involves: BALB/c) or (involves: C57BL/6)) 		abnormal digestive system development J:107620
Mapk8tm1Flv/Mapk8tm1Flv
Mapk9tm1Flv/Mapk9+
(B6.129S-Mapk9tm1Flv Mapk8tm1Flv) 		delayed intestine development J:93433
Mcm4chaos3/Mcm4Gt(RRE056)Byg
(involves: 129P2/OlaHsd * C3HeB/FeJ * C57BL/6J) 		abnormal digestive system development J:117494
Mixl1tm1.1Robb/Mixl1tm1.1Robb
(involves: 129S1/Sv) 		abnormal foregut morphology J:77443
absent hindgut J:77443
Mixl1tm1Robb/Mixl1tm1Robb
(either: (involves: 129/Sv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6)) 		abnormal foregut morphology J:77443
absent hindgut J:77443
Nckap1Gt(XE068)Byg/Nckap1Gt(XE068)Byg
(involves: 129P2/OlaHsd) 		abnormal digestive system development J:119028
Nckap1Gt(XE133)Byg/Nckap1Gt(XE133)Byg
(involves: 129P2/OlaHsd) 		abnormal digestive system development J:119028
Nckap1khlo/Nckap1khlo
(C3Fe.B6-Nckap1khlo) 		abnormal foregut morphology J:119028
Neurog3tm1Fgu/Neurog3tm3.1Ggr
Tg(Vil1-cre)20Syr/0
(involves: 129S2/SvPas * C57BL/6 * CD-1 * DBA/2 * SJL) 		abnormal intestine development J:161480
Neurog3tm3.1Ggr/Neurog3tm3.1Ggr
Tg(Vil1-cre)20Syr/0
(involves: 129S2/SvPas * C57BL/6 * CD-1 * DBA/2 * SJL) 		abnormal intestine development J:161480
Nkx2-1tm1Shk/Nkx2-1tm1Shk
(involves: 129S4/SvJae * Black Swiss) 		abnormal foregut morphology J:122531
Nkx2-3tm1Rph/Nkx2-3tm1Rph
(involves: 129S1/Sv * C57BL/6) 		delayed intestine development J:64018
Nkx3-2tm1(cre)Tsa/Nkx3-2+
Nr2f2tm2.1Tsa/Nr2f2tm2.1Tsa
(involves: 129S7/SvEvBrd * C57BL/6) 		abnormal digestive system development J:98520
NodalTgR(MPSVNeo)413.dRob/Nodaltm4Rob
(involves: 129S/SvEv * C57BL/6) 		abnormal foregut morphology J:84300
Nodaltm1Hmd/Nodal+
Tg(Rr443-Lefty1,-lacZ)36Hmd/0
(either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6N) or (involves: 129S1/Sv * 129T2/SvEms * 129X1/SvJ)) 		abnormal digestive system development J:82703
Nodaltm1Hmd/Nodaltm1Hmd
(either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6N) or (involves: 129S1/Sv * 129T2/SvEms * 129X1/SvJ)) 		abnormal digestive system development J:82703
Nodaltm1Mku/Nodaltm1.1Mku
(either: (involves: 129S1/Sv * FVB/N) or (involves: 129S1/Sv * C57BL/6J * FVB/N)) 		abnormal digestive system development J:73506
abnormal hindgut morphology J:73506
absent foregut J:73506
truncated foregut J:73506
Nogtm1Amc/Nogtm1Amc
(either: (involves: 129S1/Sv * C57BL/6) or (involves: 129S1/Sv * CD-1 * ICR)) 		abnormal esophagus development J:118341
abnormal foregut morphology J:118341
Nr6a1tm1Coo/Nr6a1tm1Coo
(involves: 129S7/SvEvBrd * C57BL/6) 		abnormal hindgut morphology J:67377
Nr6a1tm2Coo/Nr6a1tm2Coo
(involves: 129S7/SvEvBrd * C57BL/6) 		absent hindgut J:80978
Nsun2tm1a(EUCOMM)Wtsi/Nsun2tm1a(EUCOMM)Wtsi
(B6JTyr;B6N-Nsun2tm1a(EUCOMM)Wtsi/Wtsi) 		intraembryonal intestine elongation J:239583
Nubp2tm1c(EUCOMM)Hmgu/Nubp2tm1c(EUCOMM)Hmgu
H2az2Tg(Wnt1-cre)11Rth/H2az2+
Tg(Wnt1-GAL4)11Rth/0
(involves: C57BL/6) 		abnormal stomodeum morphology J:284772
Olfm4tm2.1(EGFP/cre/ERT2)Cle/Olfm4+
Znhit1tm1.1Nju/Znhit1tm1.1Nju
(involves: 129P2/OlaHsd * C57BL/6) 		abnormal intestine development J:276456
Otx2tm1Sia/Otx2tm1Sia
(involves: C57BL/6 * CBA) 		absent foregut J:29682
Ovol2tm1Xdai/Ovol2tm1Xdai
(either: (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1)) 		abnormal digestive system development J:106405
abnormal foregut morphology J:106405
abnormal hindgut morphology J:106405
Pcsk6tm1Rob/Pcsk6tm1Rob
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6) 		truncated foregut J:62181
Pdx1tm1Cvw/Pdx1tm1Cvw
(involves: 129S1/Sv * 129X1/SvJ * Black Swiss) 		abnormal foregut morphology J:32017
Pdx1tm2Cvw/Pdx1tm2Cvw
(involves: 129S1/Sv * 129X1/SvJ * Black Swiss) 		abnormal foregut morphology J:32017
Pex5tm1Baes/Pex5tm1Baes
(involves: 129S1/Sv * 129X1/SvJ) 		delayed intestine development J:42719
Pgap1oto/Pgap1oto
(involves: STOCK In(1)1Rk/J) 		truncated foregut J:41878
Pitx2tm1Jfm/Pitx2tm1Jfm
(involves: 129S4/SvJaeSor) 		abnormal digestive system development J:57674, J:69854
Pitx2tm1Jfm/Pitx2tm2.1Jfm
(involves: 129S4/SvJaeSor * C57BL/6J) 		abnormal digestive system development J:69854
Pitx2tm1Jfm/Pitx2tm2Jfm
(involves: 129S4/SvJaeSor * C57BL/6J) 		abnormal digestive system development J:69854
Pitx2tm1Kki/Pitx2tm1Kki
(involves: 129P2/OlaHsd * C57BL) 		abnormal digestive system development J:55455
Pitx2tm2.1Jfm/Pitx2tm2.1Jfm
(involves: 129S4/SvJaeSor * C57BL/6J) 		abnormal digestive system development J:69854
Prkar1atm1Gsm/Prkar1atm1Gsm
(involves: 129X1/SvJ * C57BL/6) 		abnormal foregut morphology J:78010
Psphtm1a(EUCOMM)Hmgu/Psphtm1a(EUCOMM)Hmgu
(C57BL/6N-Psphtm1a(EUCOMM)Hmgu/Wtsi) 		intraembryonal intestine elongation J:239583
Ptk2tm1Imeg/Ptk2tm1Imeg
(involves: C57BL/6 * CBA) 		abnormal foregut morphology J:29978
Pxntm1Smth/Pxntm1Smth
(either: (involves: 129S4/SvJaeSor * C57BL/6) or (involves: 129/Sv)) 		abnormal foregut morphology J:73970
Rapgef2tm1.2Hous/Rapgef2tm1.2Hous
(involves: 129S1/Sv) 		abnormal digestive system development J:165879
Rdh10trex/Rdh10trex
(involves: 129S1/Sv * C57BL/6 * FVB/NJ) 		abnormal midgut morphology J:121229
Robo1tm1Matl/Robo1tm1Matl
Robo2tm1Mrt/Robo2tm1Mrt
(involves: 129P2/OlaHsd) 		abnormal foregut morphology J:193400
Robo1tm1Matl/Robo1tm1Matl
Robo2tm1Rilm/Robo2tm1Rilm
Twist2tm1(cre)Dor/Twist2+
(involves: 129 * 129X1/SvJ) 		abnormal foregut morphology J:193400
Ror2Y324C/Ror2Y324C
(involves: C57BL/6J) 		abnormal hindgut morphology J:179805
Rprd1btm1Tshu/Rprd1btm1Tshu
Lgr5tm1(cre/ERT2)Cle/Lgr5+
Tg(Vil1-cre)20Syr/0
(involves: 129P2/OlaHsd * C57BL/6 * DBA/2) 		abnormal digestive system development J:300857
Rprd1btm1Tshu/Rprd1btm1Tshu
Tg(Vil1-cre)20Syr/0
(involves: C57BL/6 * DBA/2) 		abnormal digestive system development J:300857
Rspo2tm1Nuv/Rspo2tm1Nuv
(involves: 129 * C57BL/6) 		abnormal digestive system development J:171482
Runx1t1tm1Fc/Runx1t1+
(involves: 129S/SvEv * C57BL/6) 		absent midgut J:70590
Runx1t1tm1Fc/Runx1t1tm1Fc
(involves: 129S/SvEv * C57BL/6) 		absent midgut J:70590
Sall4tm1Brd/Sall4+
(involves: 129S7/SvEvBrd * C57BL/6J) 		persistent cloaca J:117866
Setd5tm1a(EUCOMM)Wtsi/Setd5+
(C57BL/6N-Setd5tm1a(EUCOMM)Wtsi/Wtsi) 		intraembryonal intestine elongation J:239583
Shhtm1Chg/Shhtm1Chg
(involves: 129S1/Sv * 129X1/SvJ) 		abnormal foregut morphology J:35802
Sinhcaftm1.2Hmd/Sinhcaftm1.2Hmd
(involves: 129 * C57BL/6) 		abnormal digestive system development J:313620
Sinhcaftm1Hmd/Sinhcaftm1Hmd
(involves: 129 * C57BL/6) 		abnormal digestive system development J:313620
Slc39a7tm1.1Tfk/Slc39a7tm1.1Tfk
Lgr5tm1(cre/ERT2)Cle/Lgr5+
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6) 		abnormal intestine development J:236234
Slit2tm1Matl/Slit2tm1Matl
(involves: 129S2/SvPas) 		abnormal foregut morphology J:193400
Smad2m1Mag/Smad2m1Mag
(either: (involves: 129S/Sv * Black Swiss) or (involves: 129S/Sv * C57BL/6)) 		absent foregut J:80520
Smad2tm1Cxd/Smad2+
Smad3tm1Cxd/Smad3+
(involves: 129S6/SvEvTac * NIH Black Swiss) 		abnormal foregut morphology J:106308
Smad2tm1Rob/Smad2tm2Rob
Edil3Tg(Sox2-cre)1Amc/Edil3+
(involves: 129S/SvEv * C57BL/6 * CBA * CD-1) 		truncated foregut J:84300
Smad2tm1Rob/Smad2tm2Rob
Smad3tm1Xfw/Smad3+
Edil3Tg(Sox2-cre)1Amc/Edil3+
(involves: 129/Sv * 129S/SvEv * C57BL/6 * CBA * CD-1) 		absent foregut J:84300
Smad4tm1Rob/Smad4tm1.1Rob
Edil3Tg(Sox2-cre)1Amc/Edil3+
(involves: 129S/SvEv * CD-1) 		absent foregut J:92066
absent hindgut J:92066
Smad5tm1.1Huy/Smad5tm1.1Huy
(involves: 129P2/OlaHsd) 		abnormal foregut morphology J:86157
Smad5tm1Zuk/Smad5tm1Zuk
(involves: 129S7/SvEvBrd * C57BL/6) 		abnormal digestive system development J:53293
Smotm2Amc/Smotm2Amc
Nkx3-2tm1(cre)Wez/Nkx3-2+
(involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ) 		abnormal intestine development J:199664
Sox17tm1Ysk/Sox17tm1Ysk
(involves: 129S1/Sv) 		abnormal foregut morphology J:75946
abnormal hindgut morphology J:75946
abnormal midgut morphology J:75946
Tbx6rv/Tbx6rv
(involves: C57BL/J * C57BL/6J) 		abnormal digestive system development J:8119
Tcf7l1tm2Efu/Tcf7l1tm2Efu
(involves: 129/Sv * C57BL/6) 		abnormal foregut morphology J:90402
Tcf7l2tm2.1Cle/Tcf7l2tm2.1Cle
Tg(Vil1-cre/ERT2)23Syr/0
(involves: 129P2/OlaHsd * C57BL/6 * DBA/2) 		abnormal intestine development J:185753
Tg(SRY-YFP,Tyr)TashTNpln/Tg(SRY-YFP,Tyr)TashTNpln
(involves: FVB/N) 		abnormal intestine development J:224231
Thratm1Jas/Thratm1Jas
Thrbtm1Olc/Thrbtm1Olc
(involves: 129/Sv * 129S1/Sv * 129X1/SvJ) 		delayed intestine development J:52829
Tlr4tm1.1Djh/Tlr4tm1.1Djh
(involves: C57BL/6 * FVB/N * SJL) 		abnormal enterocyte differentiation J:193668
Trim28chatwo/Trim28chatwo
(either: C57BL/6-Trim28chatwo or (involves: C57BL/6J * FVB/NJ)) 		abnormal digestive system development J:178936
Trim28tm1.1Ipc/Trim28tm1.2Ipc
Edil3Tg(Sox2-cre)1Amc/Edil3+
(involves: 129S2/SvPas * C57BL/6 * CBA) 		abnormal digestive system development J:178936
Trp63tm1Fmc/Trp63tm1Fmc
(involves: 129S4/SvJae * C57BL/6) 		abnormal esophagus development J:95347
Twsg1tm1.1Mboc/Twsg1tm1.1Mboc
(involves: 129S7/SvEvBrd * C57BL/6 * FVB/N) 		abnormal foregut morphology J:88784
Vangl2Lp/Vangl2Lp
(involves: A) 		abnormal digestive system development J:12992
Vcltm1Eda/Vcltm1Eda
(involves: 129S1/Sv * 129X1/SvJ * Black Swiss) 		abnormal foregut morphology J:45781
Wnt3avt/Wnt3avt
(involves: A * A/Gr * C57BR) 		abnormal tailgut morphology J:14984
Wnt5atm1Amc/Wnt5atm1Amc
(involves: 129S7/SvEvBrd * C57BL/6) 		abnormal digestive system development J:204986
abnormal midgut morphology J:204986
Zfp568chato/Zfp568chato
(either: (involves: 129S1/SvImJ * C57BL/6) or (involves: C3HeB/FeJ * C57BL/6) or (involves: C57BL/6 * CAST/Ei)) 		abnormal digestive system development J:139139
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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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04/30/2024
MGI 6.23 		The Jackson Laboratory