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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Mdfi
MyoD family inhibitor
MGI:107687
23 phenotypes from 1 allele in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Mdfitm1Krt/Mdfitm1Krt
B6.129S4-Mdfitm1Krt
decreased trophoblast giant cell number J:50877
embryonic growth retardation J:50877
embryonic lethality during organogenesis, complete penetrance J:50877
incomplete embryo turning J:50877
wavy neural tube J:50877
Mdfitm1Krt/Mdfitm1Krt
involves: 129S4/SvJaeSor
abnormal axial skeleton morphology J:50877
abnormal rib morphology J:50877
abnormal sclerotome morphology J:50877
abnormal sternocostal joint morphology J:50877
abnormal vertebral body morphology J:50877
abnormal vertebral spinous process morphology J:50877
curly tail J:50877
decreased body size J:50877
decreased rib number J:50877
delayed neural tube closure J:50877
kinked tail J:50877
postnatal lethality, incomplete penetrance J:50877
respiratory distress J:50877
rib bifurcation J:50877
rib fusion J:50877
spina bifida J:50877
truncated ribs J:50877
Mdfitm1Krt/Mdfitm1Krt
involves: 129S4/SvJaeSor * C57BL/6
embryonic lethality during organogenesis, incomplete penetrance J:50877

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
12/04/2018
MGI 6.13
The Jackson Laboratory