Amotl1 Phenotype Annotations

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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

Allelic Composition Genetic Background	Annotated Term	Reference
Amotl1^em1Rstot/Amotl1⁺ involves: C57BL/6J * C57BL/6N	postnatal lethality, incomplete penetrance	J:270029
Amotl1^em1Rstot/Amotl1^em1Rstot 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
Amotl1^em2Rstot/Amotl1^em2Rstot involves: C57BL/6J * C57BL/6N	no abnormal phenotype detected	J:270029
Amotl1^em3Rstot/Amotl1^em3Rstot involves: C57BL/6J * C57BL/6N	no abnormal phenotype detected	J:270029
Amotl1^tm1Laho/Amotl1^tm1Laho 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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