|
Symbol Name ID |
Mab21l2
mab-21-like 2 MGI:1346022 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcornea |
Corneal opacity |
Sclerocornea |
Cataract |
Lens subluxation |
Ectopia pupillae |
Iris coloboma |
Peters anomaly |
Chorioretinal coloboma |
Optic disc coloboma |
Optic nerve aplasia |
Morning glory anomaly |
Macular coloboma |
Retinal coloboma |
Remnants of the hyaloid vascular system |
Anophthalmia |
Microphthalmia |
Coloboma |
Strabismus |
Esotropia |
Exotropia |
Hypertropia |
Nystagmus |
Reduced visual acuity |
| Disease(s) Associated with MAB21L2 | ||||||||||||||||||||||||
| coloboma | ||||||||||||||||||||||||
| syndromic microphthalmia 14 |
| Mouse Phenotypes | abnormal retina pigment epithelium morphology |
abnormal eye morphology |
absent lens vesicle |
aphakia |
abnormal optic vesicle formation |
abnormal retina progenitor cell morphology |
microphthalmia |
abnormal retina morphology |
anophthalmia |
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| Availability | Mouse Genotype | |||||||||
| Mab21l2tm1Nao/Mab21l2tm1Nao | ||||||||||
| Mab21l2em1(IMPC)Mbp/Mab21l2+ | ||||||||||
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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