Symbol
| CELF4
| contributors: mct - updated : 13-07-2018
|
HGNC name
| CUGBP, Elav-like family member 4
|
HGNC id
| 14015
|
Other morbid association(s)
|
Type | Gene Modification | Chromosome rearrangement | Protein expression | Protein Function
|
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constitutional
|  
| deletion
|  
|  
|
with haploinsufficiency of CELF4 in syndromic intellectual disability and autism | |
Variant & Polymorphism
|
| |
Candidate gene
Marker
Therapy target
| | | |
| mice deficient for neuronal RNA-binding protein Celf4 have a complex neurological disorder with epilepsy as a prominent feature | |
altered excitatory neurotransmission resulting from Celf4 deficiency underlies the complex seizure disorder in Celf4 mutant mice |