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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Amotl1
angiomotin-like 1
MGI:1922973
7 phenotypes from 4 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Amotl1em1Rstot/Amotl1+
involves: C57BL/6J * C57BL/6N 		postnatal lethality, incomplete penetrance J:270029
Amotl1em1Rstot/Amotl1em1Rstot
involves: C57BL/6J * C57BL/6N 		normal cardiovascular system phenotype J:270029
normal craniofacial phenotype J:270029
neonatal lethality, complete penetrance J:270029
prenatal lethality, incomplete penetrance J:270029
Amotl1em2Rstot/Amotl1em2Rstot
involves: C57BL/6J * C57BL/6N 		no abnormal phenotype detected J:270029
Amotl1em3Rstot/Amotl1em3Rstot
involves: C57BL/6J * C57BL/6N 		no abnormal phenotype detected J:270029
Amotl1tm1Laho/Amotl1tm1Laho
Tg(Cdh5-cre/ERT2)1Rha/0
involves: C57BL/6 		abnormal tumor vascularization J:253854
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
04/16/2024
MGI 6.23 		The Jackson Laboratory