Selected-GenAtlas references SOURCE GeneCards NCBI Gene Swiss-Prot Orphanet Ensembl
HGNC UniGene Nucleotide OMIM UCSC
Home Page
FLASH GENE
Symbol FOXG1 contributors: mct/npt/pgu - updated : 28-03-2015
HGNC name forkhead box G1
HGNC id 3811
ASSOCIATED DISORDERS
corresponding disease(s) RTTL1 , DEL14Q12 , DEL14QP , DUP14QP
Other morbid association(s)
TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
constitutional   deletion    
in mental retardation with microcephaly
constitutional     --other  
haploinsufficiencyof FOXG1 is an emerging cause of dyskinetic encephalopathy of infancy 1)
Susceptibility to infantile spasms (ISS)
Variant & Polymorphism other CNV associated with infantile spasms (ISS)
Candidate gene
Marker
Therapy target
ANIMAL & CELL MODELS