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Symbol Name ID |
Meox1
mesenchyme homeobox 1 MGI:103220 |
| Darker colors indicate more annotations |
| Human Phenotypes | Short neck |
Fused cervical vertebrae |
Cervical C2/C3 vertebral fusion |
Sprengel anomaly |
Scoliosis |
| Disease(s) Associated with MEOX1 | |||||
| Klippel-Feil syndrome 2 |
| Mouse Phenotypes | abnormal rib development |
rib fusion |
abnormal vertebrae development |
hemivertebra |
vertebral fusion |
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| Availability | Mouse Genotype | |||||
| Meox1tm1Bmk/Meox1tm1Bmk | ||||||
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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