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FLASH GENE

Symbol

FOXG1

contributors: mct/npt/pgu - updated : 28-03-2015

HGNC name	forkhead box G1
HGNC id	3811

FLASH GENE DNA RNA EXPRESSION PROTEIN DISORDER ANIMAL & CELL MODELS

ASSOCIATED DISORDERS

corresponding disease(s)

RTTL1 , DEL14Q12 , DEL14QP , DUP14QP

Other morbid association(s)

Type Gene Modification Chromosome rearrangement Protein expression Protein 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