Ankmy2 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Ankmy2
ankyrin repeat and MYND domain containing 2
MGI:2144755

21 phenotypes from 3 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Ankmy2^em1(IMPC)Bay/Ankmy2⁺ C57BL/6N-Ankmy2^em1(IMPC)Bay/BayMmucd	abnormal embryo size	J:211773
	abnormal placenta development	J:211773
	abnormal placenta size	J:211773
	embryonic growth retardation	J:211773
	pallor	J:211773
Ankmy2^em1(IMPC)Bay/Ankmy2^em1(IMPC)Bay C57BL/6N-Ankmy2^em1(IMPC)Bay/BayMmucd	abnormal embryo development	J:211773
	abnormal embryo size	J:211773
	abnormal embryo turning	J:211773
	abnormal forebrain development	J:211773
	abnormal heart morphology	J:211773
	abnormal hindbrain development	J:211773
	abnormal midbrain development	J:211773
	abnormal neural tube closure	J:211773
	abnormal neural tube morphology	J:211773
	abnormal pharyngeal arch morphology	J:211773
	abnormal somite shape	J:211773
	abnormal vitelline vasculature morphology	J:211773
	prenatal lethality prior to heart atrial septation	J:211773
	preweaning lethality, complete penetrance	J:211773
Ankmy2^{tm1a(EUCOMM)Hmgu}/Ankmy2^{tm1a(EUCOMM)Hmgu} Edil3^{Tg(Sox2-cre)1Amc}/0 involves: C57BL/6 * C57BL/6N * CBA	abnormal embryonic neuroepithelial layer differentiation	J:297055
	embryonic lethality between somite formation and embryo turning, complete penetrance	J:297055
Ankmy2^{tm1b(EUCOMM)Hmgu}/Ankmy2^{tm1b(EUCOMM)Hmgu} involves: C57BL/6 * C57BL/6N	abnormal embryonic neuroepithelial layer differentiation	J:297055
	craniorachischisis	J:297055
	embryonic lethality between somite formation and embryo turning, complete penetrance	J:297055

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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