Amotl2 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Amotl2
angiomotin-like 2
MGI:1929286

16 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Amotl2^em1(IMPC)Mbp/Amotl2^em1(IMPC)Mbp C57BL/6NCrl-Amotl2^em1(IMPC)Mbp/MbpMmucd	abnormal cornea morphology	J:211773
	abnormal eye morphology	J:211773
	abnormal lens morphology	J:211773
	cornea opacity	J:211773
	cornea vascularization	J:211773
	decreased body length	J:211773
	decreased prepulse inhibition	J:211773
	exophthalmos	J:211773
	impaired pupillary reflex	J:211773
	increased heart weight	J:211773
	increased monocyte cell number	J:211773
	iris synechia	J:211773
Amotl2^tm1.1Laho/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
Amotl2^tm1.1Laho/Amotl2^tm1.1Laho 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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