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Symbol Name ID |
Apc
APC, WNT signaling pathway regulator MGI:88039 |
| Darker colors indicate more annotations |
| Human Phenotypes | Congenital hypertrophy of retinal pigment epithelium |
Total ophthalmoplegia |
Diplopia |
Progressive visual loss |
| Disease(s) Associated with APC | ||||
| familial adenomatous polyposis 1 | ||||
| medulloblastoma |
| Mouse Phenotypes | corneal epithelium hyperplasia |
blepharoptosis |
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| Availability | Mouse Genotype | ||
| Apctm2Rak/Apctm2Rak Tg(KRT14-cre)8Brn/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 04/16/2024 MGI 6.23 |
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