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Symbol Name ID |
Hmx1
H6 homeobox 1 MGI:107178 |
| Darker colors indicate more annotations |
| Human Phenotypes | Posterior synechiae of the anterior chamber |
Posterior embryotoxon |
Microcornea |
Sclerocornea |
Microphakia |
Cataract |
Developmental cataract |
Iris coloboma |
Iris cyst |
Ocular anterior segment dysgenesis |
Chorioretinal coloboma |
Chorioretinal atrophy |
Morning glory anomaly |
Macular hypoplasia |
Retinal coloboma |
Retinal detachment |
Cone/cone-rod dystrophy |
Rod-cone dystrophy |
Microphthalmia |
Phthisis bulbi |
Ocular hypertension |
Exodeviation |
Nystagmus |
Congenital nystagmus |
Horizontal nystagmus |
Ultra-low vision with retained light perception |
| Disease(s) Associated with HMX1 | ||||||||||||||||||||||||||
| oculoauricular syndrome |
| Mouse Phenotypes | microphthalmia |
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| Availability | Mouse Genotype | |
| Hmx1dmbo/Hmx1dmbo | ||
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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