Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 49
Gene Symbol: ACR
ACR
0.100 GeneticVariation disease BEFREE Fifty-eight offspring aged 5 to 46 years (35 males and 23 females) from 20 complete nuclear families ascertained through affected mothers with FMS were clinically evaluated for FMS according to the ACR 1990 diagnostic criteria. 8989805 1996
Entrez Id: 6863
Gene Symbol: TAC1
TAC1
0.090 AlteredExpression disease BEFREE Because former investigations have reported abnormal changes in the expression of serotonin (5-hydroxytryptamine [5-HT]) and substance P (SP) in serum and cerebrospinal fluid, this study sought to determine whether 5-HT and pain-modulating neuropeptides (SP, galanin [GA], pituitary adenylyl cyclase-activating polypeptide, and secretoneurin) were expressed abnormally in the muscle tissue of patients with fibromyalgia (FM). 9751103 1998
Entrez Id: 7857
Gene Symbol: SCG2
SCG2
0.010 AlteredExpression disease BEFREE Because former investigations have reported abnormal changes in the expression of serotonin (5-hydroxytryptamine [5-HT]) and substance P (SP) in serum and cerebrospinal fluid, this study sought to determine whether 5-HT and pain-modulating neuropeptides (SP, galanin [GA], pituitary adenylyl cyclase-activating polypeptide, and secretoneurin) were expressed abnormally in the muscle tissue of patients with fibromyalgia (FM). 9751103 1998
Entrez Id: 3356
Gene Symbol: HTR2A
HTR2A
0.060 GeneticVariation disease BEFREE The T102C polymorphism of the 5-HT2A-receptor gene in fibromyalgia. 10527809 1999
Entrez Id: 6532
Gene Symbol: SLC6A4
SLC6A4
0.050 GeneticVariation disease BEFREE A higher frequency of the S/S genotype of 5-HTT was found in FM patients compared with healthy controls. 10555044 1999
Entrez Id: 3855
Gene Symbol: KRT7
KRT7
0.010 Biomarker disease BEFREE Additionally, the psychopathologic state of 52 of the FM patients was evaluated using the Beck Depression Inventory (BDI) and the Symptom Checklist-90-Revised (SCL-90-R). 10555044 1999
Entrez Id: 51540
Gene Symbol: SCLY
SCLY
0.010 Biomarker disease BEFREE Additionally, the psychopathologic state of 52 of the FM patients was evaluated using the Beck Depression Inventory (BDI) and the Symptom Checklist-90-Revised (SCL-90-R). 10555044 1999
Entrez Id: 6886
Gene Symbol: TAL1
TAL1
0.010 Biomarker disease BEFREE Additionally, the psychopathologic state of 52 of the FM patients was evaluated using the Beck Depression Inventory (BDI) and the Symptom Checklist-90-Revised (SCL-90-R). 10555044 1999
Entrez Id: 3356
Gene Symbol: HTR2A
HTR2A
0.060 GeneticVariation disease BEFREE T102C polymorphism of the 5-HT2A receptor gene is not associated with the etiology of FS. 11732859 2001
Entrez Id: 6532
Gene Symbol: SLC6A4
SLC6A4
0.050 GeneticVariation disease LHGDN We concluded that neither 5-HTT nor its polymorphism is associated with FS. 12111622 2002
Entrez Id: 6532
Gene Symbol: SLC6A4
SLC6A4
0.050 GeneticVariation disease BEFREE We concluded that neither 5-HTT nor its polymorphism is associated with FS. 12111622 2002
Entrez Id: 7124
Gene Symbol: TNF
TNF
0.100 Biomarker disease BEFREE Detection of interleukin 1beta (IL-1beta), IL-6, and tumor necrosis factor-alpha in skin of patients with fibromyalgia. 12508404 2003
Entrez Id: 3569
Gene Symbol: IL6
IL6
0.050 GeneticVariation disease BEFREE Positive signals (RT-PCR) were detected in skin tissues of 19/50 (38%) FM patients for IL-1beta, in 14/51 FM patients (27%) for IL-6, and in 17/53 patients (32%) for TNF-a. 12508404 2003
Entrez Id: 6863
Gene Symbol: TAC1
TAC1
0.090 Biomarker disease BEFREE It summarises the current knowledge on measurements of SP in the CSF and serum in patients with depressive disorders or fibromyalgia, effects of SP-application in humans, SP-receptor expression in postmortem brains and the modulation of SP levels in the course of antidepressant treatment. 12692775 2003
Entrez Id: 1312
Gene Symbol: COMT
COMT
0.100 GeneticVariation disease BEFREE For this study, the significance of COMT polymorphism was assessed in FS. 12739038 2003
Entrez Id: 1312
Gene Symbol: COMT
COMT
0.100 GeneticVariation disease LHGDN For this study, the significance of COMT polymorphism was assessed in FS. 12739038 2003
Entrez Id: 5443
Gene Symbol: POMC
POMC
0.020 GeneticVariation disease BEFREE Fibromyalgia syndrome (FS) is associated with a neuroendocrinal disorder characterized by abnormal function of the hypothalamic-pituitary-adrenal (HPA) axis, including hyperactive adrenocorticotropic hormone (ACTH) release and adrenal hyporesponsiveness. 12739038 2003
Entrez Id: 3359
Gene Symbol: HTR3A
HTR3A
0.010 GeneticVariation disease BEFREE In our study, both serotonin receptor subunit genes, HTR3A and HTR3B, have been investigated for sequence variations in FMS patients in order to reveal a possible involvement in the aetiology of FMS. 15293096 2004
Entrez Id: 9177
Gene Symbol: HTR3B
HTR3B
0.010 Biomarker disease BEFREE Sequence variants of the serotonin receptor subunit genes HTR3A and HTR3B indicate no obvious significance in the aetiology of fibromyalgia, yet they represent the basis for future studies on their pharmacogenetic relevance. 15293096 2004
Entrez Id: 3565
Gene Symbol: IL4
IL4
0.030 GeneticVariation disease BEFREE Accordingly, the MAOA 941 position and IL-4 intron3 polymorphisms are not susceptible markers to predict FM. 16547693 2007
Entrez Id: 4128
Gene Symbol: MAOA
MAOA
0.020 GeneticVariation disease BEFREE Accordingly, the MAOA 941 position and IL-4 intron3 polymorphisms are not susceptible markers to predict FM. 16547693 2007
Entrez Id: 6863
Gene Symbol: TAC1
TAC1
0.090 Biomarker disease BEFREE The hypothesis is put forward that FMS is a neuro-immunoendocrine disorder where increased release of CRH and SP from neurons in specific muscle sites triggers local mast cells to release proinflammatory and neurosensitizing molecules. 16569342 2006
Entrez Id: 1392
Gene Symbol: CRH
CRH
0.010 Biomarker disease BEFREE The hypothesis is put forward that FMS is a neuro-immunoendocrine disorder where increased release of CRH and SP from neurons in specific muscle sites triggers local mast cells to release proinflammatory and neurosensitizing molecules. 16569342 2006
Entrez Id: 3565
Gene Symbol: IL4
IL4
0.030 AlteredExpression disease BEFREE We present here the first case in the literature with MDS/MPD syndrome, sole 5q- anomaly and thrombocytosis in which bortezomib administration normalized platelet count, produced a major erythroid response, and reduced levels of interleukin-6 (IL-6) and TNF-alpha while increased levels of IL-4 in the bone marrow plasma. 16820206 2007
Entrez Id: 4846
Gene Symbol: NOS3
NOS3
0.020 GeneticVariation disease BEFREE No evidence for an association between the Glu298Asp polymorphism of the endothelial nitric oxide synthase gene and fibromyalgia syndrome. 16951945 2007