Selected-GenAtlas references SOURCE GeneCards NCBI Gene Swiss-Prot Ensembl
HGNC UniGene Nucleotide OMIM UCSC
Home Page
FLASH GENE
Symbol CELF4 contributors: mct - updated : 13-07-2018
HGNC name CUGBP, Elav-like family member 4
HGNC id 14015
ASSOCIATED DISORDERS
corresponding disease(s)
Other morbid association(s)
TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
constitutional   deletion    
with haploinsufficiency of CELF4 in syndromic intellectual disability and autism
Susceptibility
Variant & Polymorphism
Candidate gene
Marker
Therapy target
ANIMAL & CELL MODELS
  • 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