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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Chrd
chordin
MGI:1313268
40 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background		 Annotated Term Reference
Bmpertm1Emdr/Bmpertm1Emdr
Chrdtm1Emdr/Chrdtm1Emdr
involves: 129 * C57BL/6 * SJL 		abnormal skeleton morphology J:141243
abnormal vertebral arch morphology J:141243
decreased rib number J:141243
thoracic vertebral transformation J:141243
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
Chrdtm1Emdr/Chrdtm1Emdr
Nogtm1Amc/Nogtm1Amc
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL/J 		abnormal cephalic neural fold morphology J:60303
abnormal diencephalon morphology J:60303
abnormal direction of heart looping J:60303
abnormal facial morphology J:60303
abnormal forebrain development J:60303
abnormal left-right axis patterning J:60303
abnormal mesendoderm development J:60303
abnormal telencephalon morphology J:60303
absent mandible J:60303
absent nasal placodes J:60303
absent notochord J:60303
absent sclerotome J:60303
anophthalmia J:60303
aprosencephaly J:60303
cyclopia J:60303
decreased forebrain size J:60303
embryonic lethality between somite formation and embryo turning, incomplete penetrance J:60303
embryonic lethality during organogenesis, incomplete penetrance J:60303
holoprosencephaly J:60303
lethality throughout fetal growth and development, complete penetrance J:60303
proboscis J:60303
small pharynx J:60303
tracheoesophageal fistula J:60303
Chrdtm1Emdr/Chrdtm1Emdr
Nogtm1Amc/Nogtm1Amc
involves: 129S1/Sv * 129X1/SvJ * ICR 		abnormal direction of heart looping J:137629
Chrdtm1Emdr/Chrdtm1Emdr
Smad3tm1Xfw/Smad3+
involves: 129/Sv * 129S1/Sv * 129X1/SvJ 		normal embryo phenotype J:161524
Chrdtm1Emdr/Chrdtm1Emdr
Smad3tm1Xfw/Smad3tm1Xfw
involves: 129/Sv * 129S1/Sv * 129X1/SvJ 		normal embryo phenotype J:161524
Chrdtm1Emdr/Chrdtm1Emdr
Tbx1m1Jlk/Tbx1m1Jlk
129/Sv-Tbx1m1Jlk Chrdtm1Emdr 		abnormal outer ear morphology J:146769
athymia J:146769
cleft palate J:146769
persistent truncus arteriosus J:146769
short mandible J:146769
Chrdtm1Emdr/Chrdtm1Emdr
Twsg1tm1.1Mboc/Twsg1tm1.1Mboc
involves: 129/Sv * C57BL/6 * FVB/N 		abnormal mandible morphology J:88784
abnormal vertebral arch morphology J:88784
normal nervous system phenotype J:88784
perinatal lethality J:88784
Contributing Projects:
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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Send questions and comments to User Support. 		last database update
04/09/2024
MGI 6.23 		The Jackson Laboratory