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Symbol
Name
ID
Msx2
msh homeobox 2
MGI:97169
Phenotype annotations related to growth/size/body
Darker colors indicate more annotations
Human Phenotypes
Inguinal hernia
Umbilical hernia
Disease(s) Associated with MSX2
craniosynostosis

Mouse Phenotypes
degenerate molars
ameloblast degeneration
abnormal enamel organ morphology
abnormal stellate reticulum morphology
abnormal stratum intermedium morphology
brittle teeth
malocclusion
big ears
embryonic growth retardation
Availability Mouse Genotype
Msx2tm1.1Yvla/Msx2tm1.1Yvla
Msx2tm1Rilm/Msx2tm1Rilm

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
04/16/2024
MGI 6.23
The Jackson Laboratory