Symbol Name ID |
Alx1
ALX homeobox 1 MGI:104621 |
Darker colors indicate more annotations |
Human Phenotypes | Hypertelorism |
Microphthalmia |
Disease(s) Associated with ALX1 | ||
frontonasal dysplasia 3 |
Mouse Phenotypes | increased periocular mesenchyme apoptosis |
abnormal periocular mesenchyme morphology |
abnormal optic cup morphology |
abnormal optic stalk morphology |
microphthalmia |
eyelids open at birth |
anophthalmia |
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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 04/16/2024 MGI 6.23 |
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