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Symbol Name ID |
Celf2
CUGBP, Elav-like family member 2 MGI:1338822 |
| Darker colors indicate more annotations |
| Human Phenotypes | Ventriculomegaly |
Tremor |
Hypsarrhythmia |
Delayed speech and language development |
Autistic behavior |
Stereotypical hand wringing |
Intellectual disability |
Inability to walk |
Epileptic encephalopathy |
Delayed ability to crawl |
Delayed ability to roll over |
Delayed ability to sit |
Delayed ability to walk |
Seizure |
Epileptic spasm |
| Disease(s) Associated with CELF2 | |||||||||||||||
| developmental and epileptic encephalopathy 97 |
| Mouse Phenotypes | abnormal axon extension |
abnormal neuron physiology |
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| Availability | Mouse Genotype | ||
| Celf2tm1.1Yjin/Celf2tm1.1Yjin | |||
| Celf2tm1Yjin/Celf2tm1Yjin Tg(Nes-cre)1Kln/0 (conditional) |
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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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