Amn Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Amn
amnionless
MGI:1934943

25 phenotypes from 3 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Amn^amn/Amn^amn involves: 129S1/SvImJ * C57BL/6J	abnormal ectoderm development	J:51542
	abnormal primitive streak formation	J:51542
	absent mesoderm	J:51542
	absent primitive node	J:51542
	absent somites	J:51542
	caudal body truncation	J:51542
	normal embryo phenotype	J:51542
	embryonic growth arrest	J:68615
	embryonic lethality during organogenesis, incomplete penetrance	J:51542, J:68615
Amn^amn/Amn^amn involves: C57BL/6J	abnormal ectoderm development	J:34163, J:51542
	abnormal embryonic tissue morphology	J:50810
	abnormal mesoderm development	J:34163
	abnormal nervous system development	J:34163
	abnormal primitive streak formation	J:51542
	abnormal primitive streak morphology	J:50810
	absent amnion	J:34163, J:51542
	absent mesoderm	J:51542
	absent notochord	J:34163
	absent primitive node	J:34163, J:51542
	absent somites	J:34163
	embryonic growth arrest	J:34163
	embryonic lethality during organogenesis, complete penetrance	J:34163
	increased embryonic tissue cell apoptosis	J:50810
Amn^b2b2259Clo/Amn^b2b2259Clo C57BL/6J-Amn^b2b2259Clo	abnormal left subclavian artery morphology	J:175213
	abnormal pulmonary artery morphology	J:175213
	abnormal sternum morphology	J:175213
	cardiac hypertrophy	J:175213
	double outlet right ventricle, ventricular defect committed to aorta	J:175213
	microphthalmia	J:175213
	right aortic arch	J:175213
	vascular ring	J:175213
Amn^tm1Ehl/Amn^tm1Ehl involves: 129X1/SvJ	embryonic growth arrest	J:68615
Amn^tm1Ehl/Amn^tm1Ehl involves: 129X1/SvJ	embryonic lethality during organogenesis, incomplete penetrance	J:68615

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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