|
Symbol Name ID |
Ophn1
oligophrenin 1 MGI:2151070 |
| Darker colors indicate more annotations |
| Human Phenotypes | Micropenis |
Microphallus |
Small scrotum |
Cryptorchidism |
| Disease(s) Associated with OPHN1 | ||||
| X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance |
| Mouse Phenotypes | asthenozoospermia |
decreased litter size |
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| Availability | Mouse Genotype | ||
| Ophn1Wtgr/Ophn1+ | |||
| Ophn1Wtgr/Y | |||
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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