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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Meis3
Meis homeobox 3
MGI:108519
20 phenotypes from 1 allele in 1 genetic background
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Allelic Composition
Genetic Background
Annotated Term Reference
Meis3tm1b(EUCOMM)Hmgu/Meis3tm1b(EUCOMM)Hmgu
C57BL/6N-Meis3tm1b(EUCOMM)Hmgu/Ccpcz
abnormal eye morphology J:211773
abnormal liver morphology J:211773
abnormal seminal vesicle morphology J:211773
abnormal skin morphology J:211773
abnormal spleen morphology J:211773
abnormal testis morphology J:211773
abnormal thymus morphology J:211773
abnormal tooth color J:211773
abnormal tooth morphology J:211773
abnormal urinary bladder morphology J:211773
cystolithiasis J:211773
decreased heart rate J:211773
decreased lung elastance J:211773
decreased lung tissue damping J:211773
enlarged thymus J:211773
hyperactivity J:211773
impaired glucose tolerance J:211773
microphthalmia J:211773
small liver J:211773
small testis J:211773

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
04/09/2024
MGI 6.23
The Jackson Laboratory