Symbol Name ID |
Alx3
aristaless-like homeobox 3 MGI:1277097 |
Darker colors indicate more annotations |
Human Phenotypes | Widow's peak |
Hypoplasia of the maxilla |
Hypoplastic frontal sinuses |
Anterior basal encephalocele |
Cranium bifidum occultum |
Preauricular skin tag |
Median cleft upper lip |
Median cleft palate |
Widely-spaced maxillary central incisors |
Short columella |
Bifid nasal tip |
Broad nasal tip |
Wide nasal bridge |
Bifid nose |
Epicanthus |
Disease(s) Associated with ALX3 | |||||||||||||||
frontonasal dysplasia 1 |
Mouse Phenotypes | abnormal craniofacial development |
midline facial cleft |
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Availability | Mouse Genotype | ||
Alx3tm1Hubr/Alx3tm1Hubr |
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 04/30/2024 MGI 6.23 |
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