Gene: FTL ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2512
Gene Symbol: FTL
FTL 		0.320 Biomarker group GENOMICS_ENGLAND Neuroferritinopathy. 24209436 2013
Entrez Id: 2512
Gene Symbol: FTL
FTL 		0.320 GeneticVariation group BEFREE Neuroferritinopathy is an autosomal dominant progressive movement disorder which occurs due to mutations in the ferritin light chain gene (FTL1). 22278127 2012
Entrez Id: 2512
Gene Symbol: FTL
FTL 		0.320 GeneticVariation group BEFREE Nucleotide insertions that modify the C terminus of ferritin light chain (FTL) cause neurodegenerative movement disorders named neuroferritinopathies, which are inherited with dominant transmission. 20159981 2010