|
Symbol Name ID |
Rnf168
ring finger protein 168 MGI:1917488 |
| Darker colors indicate more annotations |
| Human Phenotypes | Intraventricular hemorrhage |
Microcephaly |
Demyelinating peripheral neuropathy |
Abnormal cerebral white matter morphology |
Ataxia |
Clumsiness |
Poor hand-eye coordination |
Emotional lability |
Gait disturbance |
Headache |
Global developmental delay |
Mild global developmental delay |
Specific learning disability |
| Disease(s) Associated with RNF168 | |||||||||||||
| RIDDLE syndrome |
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 05/21/2024 MGI 6.23 |
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