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Symbol Name ID |
Cyp2u1
cytochrome P450, family 2, subfamily u, polypeptide 1 MGI:1918769 |
| Darker colors indicate more annotations |
| Human Phenotypes | Basal ganglia calcification |
| Disease(s) Associated with CYP2U1 | |
| hereditary spastic paraplegia 56 |
| Mouse Phenotypes | abnormal bone structure |
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| Availability | Mouse Genotype | |
| Cyp2u1tm1b(EUCOMM)Wtsi/Cyp2u1tm1b(EUCOMM)Wtsi | ||
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 05/19/2026 MGI 6.24 |
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