Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 26047
Gene Symbol: CNTNAP2
CNTNAP2 		0.310 Biomarker phenotype BEFREE A study of the role of the FOXP2 and CNTNAP2 genes in persistent developmental stuttering. 24807205 2014
Entrez Id: 26047
Gene Symbol: CNTNAP2
CNTNAP2 		0.310 Biomarker phenotype CTD_human Identification of a microdeletion at the 7q33-q35 disrupting the CNTNAP2 gene in a Brazilian stuttering case. 21108403 2010
Entrez Id: 29108
Gene Symbol: PYCARD
PYCARD 		0.010 Biomarker phenotype BEFREE We used TMS combined with EEG to shed light on connections in DS, stimulating the SMA. 30476712 2019
Entrez Id: 1813
Gene Symbol: DRD2
DRD2 		0.010 GeneticVariation phenotype BEFREE In the present study, we aimed to investigate the relationship between developmental stuttering in children and the levels of serum homovanillic acid (HVA), dopamine D2 receptor (DRD2) rs6277" genes_norm="1813">C957T (rs6277), and solute carrier family 6 member 3 (SLC6A3) human dopamine transporter (hDAT) A559V (rs28364997) single-nucleotide polymorphisms. 30199750 2019
Entrez Id: 7298
Gene Symbol: TYMS
TYMS 		0.010 Biomarker phenotype BEFREE We used TMS combined with EEG to shed light on connections in DS, stimulating the SMA. 30476712 2019
Entrez Id: 6531
Gene Symbol: SLC6A3
SLC6A3 		0.010 GeneticVariation phenotype BEFREE In the present study, we aimed to investigate the relationship between developmental stuttering in children and the levels of serum homovanillic acid (HVA), dopamine D2 receptor (DRD2) rs6277" genes_norm="1813">C957T (rs6277), and solute carrier family 6 member 3 (SLC6A3) human dopamine transporter (hDAT) A559V (rs28364997) single-nucleotide polymorphisms. 30199750 2019
Entrez Id: 89782
Gene Symbol: LMLN
LMLN 		0.010 GeneticVariation phenotype BEFREE Sex steroid hormones and sex hormone binding globulin levels, CYP17 MSP AI (-34T:C) and CYP19 codon 39 (Trp:Arg) variants in children with developmental stuttering. 28992603 2017
Entrez Id: 4477
Gene Symbol: MSMB
MSMB 		0.010 GeneticVariation phenotype BEFREE Sex steroid hormones and sex hormone binding globulin levels, CYP17 MSP AI (-34T:C) and CYP19 codon 39 (Trp:Arg) variants in children with developmental stuttering. 28992603 2017
Entrez Id: 4485
Gene Symbol: MST1
MST1 		0.010 GeneticVariation phenotype BEFREE Sex steroid hormones and sex hormone binding globulin levels, CYP17 MSP AI (-34T:C) and CYP19 codon 39 (Trp:Arg) variants in children with developmental stuttering. 28992603 2017
Entrez Id: 1586
Gene Symbol: CYP17A1
CYP17A1 		0.010 AlteredExpression phenotype BEFREE Sex steroid hormones and sex hormone binding globulin levels, CYP17 MSP AI (-34T:C) and CYP19 codon 39 (Trp:Arg) variants in children with developmental stuttering. 28992603 2017
Entrez Id: 84000
Gene Symbol: TMPRSS13
TMPRSS13 		0.010 GeneticVariation phenotype BEFREE Sex steroid hormones and sex hormone binding globulin levels, CYP17 MSP AI (-34T:C) and CYP19 codon 39 (Trp:Arg) variants in children with developmental stuttering. 28992603 2017
Entrez Id: 6462
Gene Symbol: SHBG
SHBG 		0.010 AlteredExpression phenotype BEFREE Sex steroid hormones and sex hormone binding globulin levels, CYP17 MSP AI (-34T:C) and CYP19 codon 39 (Trp:Arg) variants in children with developmental stuttering. 28992603 2017
Entrez Id: 1588
Gene Symbol: CYP19A1
CYP19A1 		0.010 GeneticVariation phenotype BEFREE Sex steroid hormones and sex hormone binding globulin levels, CYP17 MSP AI (-34T:C) and CYP19 codon 39 (Trp:Arg) variants in children with developmental stuttering. 28992603 2017
Entrez Id: 23431
Gene Symbol: AP4E1
AP4E1 		0.010 GeneticVariation phenotype BEFREE Whole-exome sequencing identified two heterozygous AP4E1 coding variants, c.1549G>A (p.Val517Ile) and c.2401G>A (p.Glu801Lys), that co-segregate with persistent developmental stuttering in a large Cameroonian family, and we observed the same two variants in unrelated Cameroonians with persistent stuttering. 26544806 2015