Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1120
Gene Symbol: CHKB
CHKB
0.340 GeneticVariation disease BEFREE This comprehensive genetic study sought to assess variations in CHKB and CPT1B susceptibility genes and HLA-DQB1*06:02 allele status in Turkish patients with narcolepsy and healthy persons. 24571861 2014
Entrez Id: 1120
Gene Symbol: CHKB
CHKB
0.340 GeneticVariation disease BEFREE Chinese narcolepsy was strongly and dose dependently associated with TCRA (rs1154155C) and P2RY11 (rs2305795A) but not CPT1B/CHKB (rs5770917C) polymorphisms. 22177342 2012
Entrez Id: 1120
Gene Symbol: CHKB
CHKB
0.340 GeneticVariation disease BEFREE These studies have identified four gene variants associated with restless legs syndrome (BTBD9, MEIS1, MAP2K5/LBXCOR1, and PTPRD) and two variants associated with narcolepsy (one in the T-cell receptor α locus and another between CPT1B and CHKB). 21285061 2011
Entrez Id: 1120
Gene Symbol: CHKB
CHKB
0.340 Biomarker disease CTD_human Real-time quantitative PCR assays in white blood cells indicated decreased CPT1B and CHKB expression in subjects with the C allele, suggesting that a genetic variant regulating CPT1B or CHKB expression is associated with narcolepsy. 18820697 2008
Entrez Id: 1120
Gene Symbol: CHKB
CHKB
0.340 AlteredExpression disease BEFREE Real-time quantitative PCR assays in white blood cells indicated decreased CPT1B and CHKB expression in subjects with the C allele, suggesting that a genetic variant regulating CPT1B or CHKB expression is associated with narcolepsy. 18820697 2008