|
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 |
Prominent glabella |
Cleft palate |
Underdeveloped nasal alae |
Wide nasal bridge |
Absent eyebrow |
Sparse eyelashes |
Upper eyelid coloboma |
Tessier cleft |
| Disease(s) Associated with ALX1 | |||||||||
| frontonasal dysplasia 3 |
| Mouse Phenotypes | craniofacial 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 lateral nasal prominence morphology |
abnormal nasal capsule morphology |
midface hypoplasia |
short face |
midline cleft upper lip |
short philtrum |
cleft palate |
abnormal external nares morphology |
broad nasal bridge |
depressed nasal bridge |
abnormal nasal cartilage morphology |
short snout |
shortened head |
|
| 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) |
||
|
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 04/23/2024 MGI 6.23 |
|
|
|
||
Analysis Tools