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Symbol Name ID |
Aptx
aprataxin MGI:1913658 |
| Darker colors indicate more annotations |
| Human Phenotypes | Scoliosis |
| Disease(s) Associated with APTX | |
| ataxia with oculomotor apraxia type 1 |
| Mouse Phenotypes | decreased bone mineral content |
decreased bone mineral density |
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| Availability | Mouse Genotype | ||
| Aptxtm1b(EUCOMM)Hmgu/Aptxtm1b(EUCOMM)Hmgu | |||
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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