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Symbol Name ID |
Atg5
autophagy related 5 MGI:1277186 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Horizontal nystagmus |
| Disease(s) Associated with ATG5 | |
| autosomal recessive spinocerebellar ataxia 25 |
| Mouse Phenotypes | vision/eye phenotype |
decreased a-wave amplitude |
decreased b-wave amplitude |
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| Availability | Mouse Genotype | |||
| Atg5tm1Nmz/Atg5tm1Nmz | * | |||
| Atg5tm1Myok/Atg5tm1Myok Tg(BEST1-cre)1Taf/0 (conditional) |
* | |||
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 04/09/2024 MGI 6.23 |
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