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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Amotl2
angiomotin-like 2
MGI:1929286
6 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Amotl2em1(IMPC)Mbp/Amotl2em1(IMPC)Mbp
C57BL/6NCrl-Amotl2em1(IMPC)Mbp/MbpMmucd
abnormal eye morphology J:211773
decreased body length J:211773
Amotl2tm1.1Laho/Amotl2+
Tg(Cdh5-cre/ERT2)1Rha/0
involves: C57BL/6
abnormal aorta morphology J:226656
abnormal vascular endothelial cell morphology J:226656
aorta stenosis J:226656
Amotl2tm1.1Laho/Amotl2tm1.1Laho
Tg(Cdh5-cre/ERT2)1Rha/0
involves: C57BL/6
abnormal aorta morphology J:226656
abnormal vascular endothelial cell morphology J:226656
aorta stenosis J:226656
normal cardiovascular system phenotype J:226656

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
06/12/2024
MGI 6.13
The Jackson Laboratory