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Symbol Name ID |
Alx1
ALX homeobox 1 MGI:104621 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Brachycephaly |
| Disease(s) Associated with ALX1 | |
| frontonasal dysplasia 3 |
| Mouse Phenotypes | skeleton phenotype |
decreased cranium length |
small frontal bone |
absent interparietal bone |
small supraoccipital bone |
small parietal bone |
small alisphenoid bone |
absent presphenoid bone |
presphenoid bone hypoplasia |
small temporal bone squamous part |
absent neurocranium |
short mandible |
abnormal maxillary shelf morphology |
premaxilla hypoplasia |
short maxilla |
abnormal palatine bone morphology |
short zygomatic bone |
acrania |
abnormal nasal capsule morphology |
abnormal nasal cartilage morphology |
abnormal pectoral girdle bone morphology |
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| Availability | Mouse Genotype | |||||||||||||||||||||
| Alx1em1Jian/Alx1em1Jian | ||||||||||||||||||||||
| Alx1tm1Crm/Alx1tm1Crm | * | |||||||||||||||||||||
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 04/23/2024 MGI 6.23 |
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