Meox2 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Meox2
mesenchyme homeobox 2
MGI:103219

19 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Meox2^fla/Meox2^fla involves: C3HeB/FeJ * C57BL/6J	abnormal gastrocnemius morphology	J:123197
	abnormal skeletal muscle morphology	J:123197
	joint contracture	J:123197
	normal skeleton phenotype	J:123197
	thin myocardium	J:123197
	thin myometrium	J:123197
Meox2^tm1Vpa/Meox2^tm1Vpa involves: 129P2/OlaHsd	abnormal skeletal muscle morphology	J:98439
Meox2^tm1Vpa/Meox2^tm1Vpa involves: 129P2/OlaHsd	normal muscle phenotype	J:98439
Meox2^tm1Vpa/Meox2^tm1Vpa involves: 129P2/OlaHsd * C57BL/6	abnormal gait	J:56172
	abnormal limb morphology	J:56172
	abnormal limb posture	J:56172
	abnormal muscle development	J:56172
	abnormal myogenesis	J:56172
	centrally nucleated skeletal muscle fibers	J:56172
	cleft secondary palate	J:56172
	decreased skeletal muscle mass	J:56172
	decreased survivor rate	J:56172
	increased variability of skeletal muscle fiber size	J:56172
	limb grasping	J:56172
	postnatal lethality, incomplete penetrance	J:56172

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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