Mab21l2 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Mab21l2
mab-21-like 2
MGI:1346022

22 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Mab21l2^em1(IMPC)Mbp/Mab21l2⁺ C57BL/6N-Mab21l2^em1(IMPC)Mbp/Ucd	abnormal eye morphology	J:211773
	abnormal neural tube morphology	J:211773
	abnormal placenta morphology	J:211773
	abnormal placenta vasculature	J:211773
	anophthalmia	J:211773
	decreased circulating creatinine level	J:211773
	embryonic growth retardation	J:211773
	microphthalmia	J:211773
	no spontaneous movement	J:211773
Mab21l2^em1(IMPC)Mbp/Mab21l2^em1(IMPC)Mbp C57BL/6N-Mab21l2^em1(IMPC)Mbp/Ucd	abnormal heart morphology	J:211773
	prenatal lethality prior to heart atrial septation	J:211773
	preweaning lethality, complete penetrance	J:211773
Mab21l2^tm1Nao/Mab21l2^tm1Nao involves: 129 * C57BL/6	abnormal heart position or orientation	J:93910
	abnormal optic vesicle formation	J:93910
	abnormal retina morphology	J:93910
	abnormal retina pigment epithelium morphology	J:93910
	abnormal retina progenitor cell morphology	J:93910
	abnormal ventral body wall morphology	J:93910
	absent lens vesicle	J:93910
	aphakia	J:93910
	lethality throughout fetal growth and development, complete penetrance	J:93910
	omphalocele	J:93910

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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