Symbol Name ID |
Cyfip2
cytoplasmic FMR1 interacting protein 2 MGI:1924134 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Microcephaly |
Spasticity |
Ventriculomegaly |
Cerebral atrophy |
Cerebellar atrophy |
EEG with burst suppression |
Hypsarrhythmia |
Absent speech |
Hyperreflexia |
Epileptic encephalopathy |
Seizure |
Disease(s) Associated with CYFIP2 | |||||||||||
developmental and epileptic encephalopathy 65 |
Mouse Phenotypes | nervous system phenotype |
abnormal hindbrain morphology |
abnormal dendritic spine morphology |
decreased miniature excitatory postsynaptic current frequency |
increased prepulse inhibition |
|
Availability | Mouse Genotype | |||||
Cyfip2M1N/Cyfip2M1N | ||||||
Cyfip2tm1a(EUCOMM)Wtsi/Cyfip2tm1a(EUCOMM)Wtsi | ||||||
Cyfip2tm1(KOMP)Vlcg/Cyfip2+ | * |
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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