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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Fbn2
fibrillin 2
MGI:95490
6 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
Bmp7tm1Rob/Bmp7+
Fbn2tm1Rmz/Fbn2+
either: (involves: 129/Sv * 129S/SvEv) or (involves: 129/Sv * 129S/SvEv * C57BL/6J)
polysyndactyly J:70592
Fbn1tm1.2Lysa/Fbn1+
Fbn2tm1Rmz/Fbn2tm1Rmz
involves: 129/Sv * C57BL/6
neonatal lethality, incomplete penetrance J:165897
prenatal lethality, incomplete penetrance J:165897
Fbn1tm3Rmz/Fbn1+
Fbn2tm1Rmz/Fbn2tm1Rmz
involves: 129
abnormal aorta tunica media morphology J:110586
lethality throughout fetal growth and development, incomplete penetrance J:110586
Fbn1tm3Rmz/Fbn1tm3Rmz
Fbn2tm1Rmz/Fbn2tm1Rmz
involves: 129
abnormal aorta tunica media morphology J:110586
lethality throughout fetal growth and development, complete penetrance J:110586

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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last database update
06/04/2019
MGI 6.14
The Jackson Laboratory