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Symbol Name ID |
Pik3r1
phosphoinositide-3-kinase regulatory subunit 1 MGI:97583 |
| Darker colors indicate more annotations |
| Human Phenotypes | Abnormal anterior chamber morphology |
Posterior embryotoxon |
Megalocornea |
Astigmatism |
Corneal opacity |
Cataract |
Abnormal pupil morphology |
Hypoplasia of the iris |
Rieger anomaly |
Deeply set eye |
Hypertelorism |
Esotropia |
Hypermetropia |
High hypermetropia |
Myopia |
Glaucoma |
| Disease(s) Associated with PIK3R1 | ||||||||||||||||
| SHORT syndrome |
| Mouse Phenotypes | abnormal retina cone cell morphology |
retina cone cell degeneration |
decreased b-wave amplitude |
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| Availability | Mouse Genotype | |||
| Pik3r1tm1Lca/Pik3r1tm1Lca Tg(OPN1LW-cre)4Yzl/0 (conditional) |
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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 04/09/2024 MGI 6.23 |
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