Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
0.800 CausalMutation disease CLINVAR
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
0.800 Biomarker disease CTD_human
Entrez Id: 859
Gene Symbol: CAV3
CAV3
0.550 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 34
Gene Symbol: ACADM
ACADM
0.400 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 8929
Gene Symbol: PHOX2B
PHOX2B
0.350 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 54738
Gene Symbol: FEV
FEV
0.320 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 7428
Gene Symbol: VHL
VHL
0.200 Biomarker disease MGD
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
0.160 GeneticVariation disease CLINVAR
Entrez Id: 256297
Gene Symbol: PTF1A
PTF1A
0.010 GeneticVariation disease BEFREE <b>Abbreviations</b>: HAS, Haute Autorité de Santé: French National Health Authority; NICHD, National Institute of Child Health and Human Development; PACA, Provence-Alpes-Côte d'Azur region of France; SUID, sudden unexpected infant death; SIDS, sudden infant death syndrome; CépiDc, Centre d'Epidémiologie sur les Causes Médicales de Décès/Center for Epidemiology on the Medical Causes of Death. 30382004 2019
Entrez Id: 6532
Gene Symbol: SLC6A4
SLC6A4
0.800 GeneticVariation disease LHGDN 3' UTR polymorphism of the serotonin transporter gene and sudden infant death syndrome: haplotype analysis. 16691588 2006
Entrez Id: 6532
Gene Symbol: SLC6A4
SLC6A4
0.800 Biomarker disease BEFREE 5-HT neuron count and density, 5-HT(1A) receptor binding density, and 5-HT transporter (5-HTT) binding density in the medullary 5-HT system; correlation between these markers and 6 recognized risk factors for SIDS. 17077377 2006
Entrez Id: 3350
Gene Symbol: HTR1A
HTR1A
0.010 Biomarker disease BEFREE 5-HT neuron count and density, 5-HT(1A) receptor binding density, and 5-HT transporter (5-HTT) binding density in the medullary 5-HT system; correlation between these markers and 6 recognized risk factors for SIDS. 17077377 2006
Entrez Id: 3423
Gene Symbol: IDS
IDS
0.090 Biomarker disease BEFREE 6 infants (index cases) from five different families had a near-miss sudden infant death syndrome event between 3 and 12 weeks of age and had polygraphically documented apnoeas during sleep.4 of their siblings had died of SIDS. 2868338 1986
Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3
0.010 GeneticVariation disease BEFREE Sudden infant death in a patient with FGFR3 P250R mutation. 17103449 2006
Entrez Id: 54738
Gene Symbol: FEV
FEV
0.320 GeneticVariation disease LHGDN Sudden infant death syndrome: rare mutation in the serotonin system FEV gene. 17597646 2007
Entrez Id: 110806262
Gene Symbol: LOC110806262
LOC110806262
0.060 GeneticVariation disease BEFREE Sudden infant death syndrome and sudden intrauterine unexplained death: correlation between hypoplasia of raphé nuclei and serotonin transporter gene promoter polymorphism. 19342987 2009
Entrez Id: 8624
Gene Symbol: PSMG1
PSMG1
0.040 Biomarker disease BEFREE SIDS compared to non-SIDS had higher PACAP in the MBDR (p<0.05) and lower PAC1 in the medulla arcuate nucleus (p<0.001). 28392470 2017
Entrez Id: 117
Gene Symbol: ADCYAP1R1
ADCYAP1R1
0.040 Biomarker disease BEFREE SIDS compared to non-SIDS had higher PACAP in the MBDR (p<0.05) and lower PAC1 in the medulla arcuate nucleus (p<0.001). 28392470 2017
Entrez Id: 1844
Gene Symbol: DUSP2
DUSP2
0.040 Biomarker disease BEFREE SIDS compared to non-SIDS had higher PACAP in the MBDR (p<0.05) and lower PAC1 in the medulla arcuate nucleus (p<0.001). 28392470 2017
Entrez Id: 1316
Gene Symbol: KLF6
KLF6
0.040 Biomarker disease BEFREE SIDS compared to non-SIDS had higher PACAP in the MBDR (p<0.05) and lower PAC1 in the medulla arcuate nucleus (p<0.001). 28392470 2017
Entrez Id: 6476
Gene Symbol: SI
SI
0.010 Biomarker disease BEFREE SID is a condition in which sucrase-isomaltase, an enzyme produced by brush border of small intestine to metabolize sucrose, is deficient. 31493040 2020
Entrez Id: 7433
Gene Symbol: VIPR1
VIPR1
0.020 Biomarker disease BEFREE HVR1 substitutions in SIDS victims are hereditary and not due to somatic mutations. 12434891 2002
Entrez Id: 7422
Gene Symbol: VEGFA
VEGFA
0.020 Biomarker disease LHGDN Vascular endothelial growth factor in the cerebrospinal fluid of infants who died of sudden infant death syndrome: evidence for antecedent hypoxia. 12563064 2003
Entrez Id: 3586
Gene Symbol: IL10
IL10
0.100 GeneticVariation disease BEFREE Interleukin 10 genotype as a risk factor for sudden infant death syndrome: determination of IL-10 genotype from wax-embedded postmortem samples. 15325405 2004
Entrez Id: 3586
Gene Symbol: IL10
IL10
0.100 GeneticVariation disease LHGDN Interleukin 10 genotype as a risk factor for sudden infant death syndrome: determination of IL-10 genotype from wax-embedded postmortem samples. 15325405 2004