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Symbol Name ID |
Msx2
msh homeobox 2 MGI:97169 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Feeding difficulties in infancy |
Autism |
| Disease(s) Associated with MSX2 | ||
| craniosynostosis |
| Mouse Phenotypes | behavior/neurological phenotype |
tonic seizures |
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| Availability | Mouse Genotype | ||
| Msx2tm1Rilm/Msx2tm1Rilm | * | ||
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 |
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