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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Nodal
nodal growth differentiation factor
MGI:97359
75 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
Acvr1btm1Enl/Acvr1b+
Gdf1tm1Sjl/Gdf1+
Nodaltm1Rob/Nodal+
involves: 129/Sv * C57BL/6
abnormal forebrain morphology J:108723
abnormal nasal septum morphology J:108723
Acvr1ctm1Cfi/Acvr1c+
Gdf1tm1Sjl/Gdf1+
Nodaltm1Rob/Nodal+
involves: 129 * C57BL/6
no abnormal phenotype detected J:108723
Acvr1ctm1Cfi/Acvr1ctm1Cfi
Nodaltm1Rob/Nodal+
involves: 129P2/OlaHsd * 129/Sv
normal mortality/aging J:94135
Acvr2atm1Hsch/Acvr2atm1Hsch
Nodaltm1Rob/Nodal+
involves: 129S/SvEv * 129S1/Sv * C57BL/6J
abnormal gastrulation J:57262
abnormal head morphology J:57262
cyclopia J:57262
decreased forebrain size J:57262
embryonic lethality, complete penetrance J:57262
Cer1tm1Bhr/Cer1tm1Bhr
Lefty1tm1Hmd/Lefty1tm1Hmd
Nodaltm1Rob/Nodal+
involves: 129P2/OlaHsd * 129S/SvEv * 129S7/SvEvBrd * CD-1
abnormal developmental patterning J:81339
abnormal embryo development J:81339
abnormal embryonic tissue morphology J:81339
abnormal embryonic-extraembryonic boundary morphology J:81339
Cer1tm1Bhr/Cer1tm1Bhr
Lefty1tm1Sla/Lefty1tm1Sla
Nodaltm1Rob/Nodal+
involves: 129S/SvEv * 129S7/SvEvBrd * CD-1
abnormal developmental patterning J:81339
abnormal embryo development J:81339
abnormal embryonic tissue morphology J:81339
abnormal embryonic-extraembryonic boundary morphology J:81339
Chrdtm1Emdr/Chrdtm1Emdr
Nodaltm1Rob/Nodal+
involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ
abnormal anterior definitive endoderm morphology J:161524
abnormal direction of heart looping J:161524
abnormal embryonic tissue morphology J:161524
abnormal mesendoderm development J:161524
abnormal prechordal plate morphology J:161524
fused first pharyngeal arch J:161524
holoprosencephaly J:161524
Col2a1tm1.1Ksec/Col2a1+
Nodaltm1Rob/Nodal+
involves: 129S/SvEv * 129X1/SvJ * C57BL/6
abnormal head morphology J:163739
Col2a1tm1.1Ksec/Col2a1tm1.1Ksec
Nodaltm1Rob/Nodal+
involves: 129S/SvEv * 129X1/SvJ * C57BL/6
abnormal head morphology J:163739
Dand5tm1Belo/Dand5tm1Belo
Nodaltm1.1Mku/Nodal+
involves: 129/Ola * C57BL/6J
abnormal direction of heart looping J:93051
Drap1tm1Mms/Drap1tm1Mms
Nodaltm1Rob/Nodal+
involves: 129S/SvEv * 129S6/SvEvTac
abnormal gastrulation J:80667
abnormal primitive streak formation J:80667
embryonic lethality, complete penetrance J:80667
Eomestm1.1Rob/Eomes+
Nodaltm1Rob/Nodal+
involves: 129S/SvEv * 129S7/SvEvBrd * C57BL/6 * CBA
abnormal amniotic cavity morphology J:131055
abnormal anterior visceral endoderm cell migration J:131055
abnormal developmental patterning J:131055
abnormal germ layer development J:131055
abnormal left-right axis patterning J:131055
abnormal notochord morphology J:131055
abnormal primitive node morphology J:131055
abnormal rostral-caudal patterning of the somites J:131055
disorganized embryonic tissue J:131055
embryonic-extraembryonic boundary constriction J:131055
enlarged floor plate J:131055
failure of primitive streak formation J:131055
increased somite number J:131055
rostral body truncation J:131055
rostral-caudal axis duplication J:131055
Eomestm1.1Rob/Eomes+
Nodaltm4Rob/Nodaltm4Rob
involves: 129S/SvEv * C57BL/6 * CBA
no abnormal phenotype detected J:131055
Eomestm1Rob/Eomes+
Nodaltm1Rob/Nodal+
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S/SvEv * C57BL/6 * CBA
prenatal lethality J:131055
rostral body truncation J:131055
Foxa2tm1Jrt/Foxa2+
Nodaltm1Rob/Nodal+
involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ
abnormal direction of embryo turning J:32935
delayed embryo turning J:32935
situs ambiguus J:32935
Gdf1tm1Sjl/Gdf1tm1Sjl
Nodaltm1Rob/Nodal+
involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6
abnormal diencephalon morphology J:108723
abnormal first pharyngeal arch morphology J:108723
abnormal foregut morphology J:108723
abnormal mesendoderm development J:108723
abnormal neural fold formation J:108723
abnormal neural plate morphology J:108723
abnormal third ventricle morphology J:108723
absent mandible J:108723
absent notochord J:108723
absent prechordal plate J:108723
absent tongue J:108723
cleft upper lip J:108723
embryonic lethality during organogenesis, incomplete penetrance J:108723
fused first pharyngeal arch J:108723
holoprosencephaly J:108723
nasal septum hypoplasia J:108723
truncated notochord J:108723
Lefty2tm1Hmd/Lefty2tm1Hmd
Nodaltm1Rob/Nodal+
involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6Cr
abnormal embryo development J:57907
embryonic lethality between implantation and somite formation, complete penetrance J:57907
Nodaltm1.1Dbc/Nodaltm1.1Dbc
involves: 129S/SvEv * C57BL/6
abnormal mesendoderm development J:112799
abnormal primitive streak formation J:112799
embryonic growth arrest J:112799
embryonic lethality between implantation and somite formation, complete penetrance J:112799
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 cardiac outflow tract development J:82703
abnormal digestive system development J:82703
abnormal left-right axis patterning J:82703
abnormal liver morphology J:82703
dextrocardia J:82703
right atrial isomerism J:82703
right pulmonary isomerism J:82703
right-sided isomerism J:82703
small spleen J:82703
Nodaltm1Rob/Nodal+
Nogtm1Amc/Nogtm1Amc
involves: 129S/SvEv * 129S1/Sv
normal embryo phenotype J:161524
Nodaltm1Rob/Nodal+
Zic2Ku/Zic2Ku
129S.Cg-Nodaltm1Rob Zic2Ku
rostral body truncation J:238567
Nodaltm1Rob/Nodal+
Edil3Tg(Sox2-cre)1Amc/Edil3+
Tgif1tm1Caw/Tgif1tm1Caw
Tgif2tm1Dwot/Tgif2tm1Dwot
involves: 129S/SvEv * C57BL/6 * C57BL/6J * CBA
abnormal embryonic neuroepithelium morphology J:183402
abnormal forebrain development J:183402
abnormal left-right axis patterning J:157256
normal cardiovascular system phenotype J:157256
decreased forebrain size J:183402
embryonic growth retardation J:183402
holoprosencephaly J:183402
rostral body truncation J:183402
Nodaltm1Rob/Nodal+
Tgif1tm1Dwot/Tgif1tm1Dwot
Tgif2tm1Dwot/Tgif2tm1Dwot
involves: 129S/SvEv * 129X1/SvJ * C57BL/6
normal embryo phenotype J:157256
Nodaltm1Rob/Nodal+
Smad2tm1.1Epb/Smad2+
involves: 129S/SvEv * 129X1/SvJ * C57BL/6J * SJL
abnormal eye development J:183402
abnormal olfactory epithelium morphology J:183402
embryonic growth retardation J:183402
holoprosencephaly J:183402
proboscis J:183402
Nodaltm1Rob/Nodal+
Trim33tm1.2Los/Trim33tm1.2Los
involves: 129S/SvEv * 129S2/SvPas * C57BL/6
normal embryo phenotype J:163858
expanded anterior visceral endoderm J:163858
Nodaltm1Rob/Nodaltm2Rob
Trim33tm1.2Los/Trim33tm1.2Los
involves: 129S/SvEv * 129S2/SvPas * C57BL/6
normal embryo phenotype J:163858
Nodaltm2Rob/Nodal+
Zic2Ku/Zic2Ku
129S.Cg-Nodaltm2Rob Zic2Ku
abnormal mesendoderm development J:238567
rostral body truncation J:238567
Nodaltm2Rob/Nodaltm2Rob
Zic2Ku/Zic2+
129S.Cg-Nodaltm2Rob Zic2Ku
rostral body truncation J:238567
Nodaltm2Rob/Nodaltm2Rob
Zic2Ku/Zic2Ku
129S.Cg-Nodaltm2Rob Zic2Ku
rostral body truncation J:238567
Smad2tm1Enl/Smad2+
Nodaltm1Rob/Nodal+
involves: 129S/SvEv * 129S4/SvJae
abnormal craniofacial morphology J:48467
abnormal direction of embryo turning J:48467
abnormal gastrulation J:48467
abnormal heart looping J:48467
abnormal lateral plate mesoderm morphology J:48467
abnormal left-right axis patterning J:48467
cyclopia J:48467
right pulmonary isomerism J:48467
rostral body truncation J:48467
transposition of great arteries J:48467

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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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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory