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Symbol Name ID |
Uchl1
ubiquitin carboxy-terminal hydrolase L1 MGI:103149 |
| Darker colors indicate more annotations |
| Human Phenotypes | Ankle clonus |
Flexion contracture |
Pectus carinatum |
| Disease(s) Associated with UCHL1 | |||
| hereditary spastic paraplegia 79B |
| Mouse Phenotypes | abnormal spine curvature |
kyphosis |
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| Availability | Mouse Genotype | ||
| Uchl1tm1Dgen/Uchl1tm1Dgen | |||
| Uchl1tm1b(EUCOMM)Hmgu/Uchl1+ | |||
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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