Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 114781
Gene Symbol: BTBD9
BTBD9
CUI: C0035258
Disease: Restless Legs Syndrome
Restless Legs Syndrome
0.700 GeneticVariation GWASCAT Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis. 29029846

2017

Entrez Id: 114781
Gene Symbol: BTBD9
BTBD9
CUI: C0035258
Disease: Restless Legs Syndrome
Restless Legs Syndrome
0.700 GeneticVariation GWASCAT Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1. 21779176

2012

Entrez Id: 114781
Gene Symbol: BTBD9
BTBD9
CUI: C0035258
Disease: Restless Legs Syndrome
Restless Legs Syndrome
0.700 GeneticVariation GWASCAT In an Icelandic discovery sample of patients with RLS and periodic limb movements in sleep, we observed a genomewide significant association with a common variant in an intron of BTBD9 on chromosome 6p21.2 (odds ratio, 1.8; P=2x10(-9)). 17634447

2007

Entrez Id: 114781
Gene Symbol: BTBD9
BTBD9
CUI: C0035258
Disease: Restless Legs Syndrome
Restless Legs Syndrome
0.700 GeneticVariation GWASCAT In a genome-wide association study we found highly significant associations between RLS and intronic variants in the homeobox gene MEIS1, the BTBD9 gene encoding a BTB(POZ) domain as well as variants in a third locus containing the genes encoding mitogen-activated protein kinase MAP2K5 and the transcription factor LBXCOR1 on chromosomes 2p, 6p and 15q, respectively. 17637780

2007