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 |
|
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 05/28/2024 MGI 6.13 |
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