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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Meis2
Meis homeobox 2
MGI:108564
21 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+
Meis2tm1.1Zkoz/Meis2tm1.1Zkoz
Tfap2atm1(cre)Moon/Tfap2a+
involves: 129 * C57BL/6J
abnormal cardiac neural crest cell morphology J:229604
abnormal cardiac outflow tract development J:229604
abnormal cartilage morphology J:229604
abnormal facial nerve morphology J:229604
abnormal heart valve morphology J:229604
abnormal hyoid bone morphology J:229604
abnormal mandible morphology J:229604
abnormal otic capsule morphology J:229604
abnormal palate morphology J:229604
abnormal parietal bone morphology J:229604
abnormal tongue morphology J:229604
abnormal trigeminal nerve morphology J:229604
abnormal vestibulocochlear nerve morphology J:229604
absent interparietal bone J:229604
decreased cornea thickness J:229604
decreased tongue size J:229604
double outlet right ventricle J:229604
failure of eyelid fusion J:229604
neonatal lethality, complete penetrance J:229604
short mandible J:229604
small trigeminal ganglion J:229604

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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last database update
01/21/2020
MGI 6.14
The Jackson Laboratory