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Symbol Name ID |
Msx1
msh homeobox 1 MGI:97168 |
| Darker colors indicate more annotations |
| Human Phenotypes | Aplasia of the maxilla |
Enamel hypoplasia |
| Disease(s) Associated with MSX1 | ||
| tooth agenesis |
| Mouse Phenotypes | abnormal metopic suture morphology |
abnormal cranium morphology |
large anterior fontanelle |
abnormal frontal bone morphology |
overlapping parietal bones |
absent alveolar process |
abnormal tooth morphology |
absent incisors |
absent lower incisors |
absent upper incisors |
absent molars |
growth retardation of molars |
abnormal mandible morphology |
cleft chin |
short mandible |
absent maxillary shelf |
absent premaxilla |
short maxilla |
small nasal bone |
absent palatine bone horizontal plate |
absent malleus processus brevis |
short malleus |
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| Availability | Mouse Genotype | ||||||||||||||||||||||
| Msx1tm1Bero/Msx1tm1Bero | |||||||||||||||||||||||
| Msx1tm1Rilm/Msx1tm1Rilm | |||||||||||||||||||||||
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 |
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