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Symbol Name ID |
Cit
citron MGI:105313 |
| Darker colors indicate more annotations |
| Human Phenotypes | Delayed early-childhood social milestone development |
| Disease(s) Associated with CIT | |
| primary autosomal recessive microcephaly 17 |
| Mouse Phenotypes | increased susceptibility to pharmacologically induced seizures |
tremors |
ataxia |
abnormal gait |
myoclonus |
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| Availability | Mouse Genotype | |||||
| Cittm1Fdc/Cittm1Fdc | ||||||
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 04/23/2024 MGI 6.23 |
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