SOX17, SRY-box transcription factor 17, 64321

N. diseases: 113; N. variants: 2
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3150927
Disease: VESICOURETERAL REFLUX 3
VESICOURETERAL REFLUX 3
0.600 GeneticVariation disease UNIPROT Mutations in SOX17 are associated with congenital anomalies of the kidney and the urinary tract. 20960469 2010
CUI: C0042580
Disease: Vesico-Ureteral Reflux
Vesico-Ureteral Reflux
0.410 GeneticVariation disease BEFREE We have identified mutations in SOX17, an HMG-box transcription factor and Wnt signaling antagonist, in eight patients with CAKUT (seven vesico-ureteric reflux, one pelvic obstruction). 20960469 2010
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma
0.050 GeneticVariation disease BEFREE We identified networks regulated by known cancer drivers such as GATA3 and FOXA1 (breast cancer), SOX17 and FOXA2 (endometrial cancer), and NFE2L2, SOX2, and TP63 (squamous cell lung cancer). 25994056 2015
CUI: C0007103
Disease: Malignant neoplasm of endometrium
Malignant neoplasm of endometrium
0.040 GeneticVariation disease BEFREE We identified networks regulated by known cancer drivers such as GATA3 and FOXA1 (breast cancer), SOX17 and FOXA2 (endometrial cancer), and NFE2L2, SOX2, and TP63 (squamous cell lung cancer). 25994056 2015
CUI: C0007766
Disease: Intracranial Aneurysm
Intracranial Aneurysm
0.040 GeneticVariation disease BEFREE However, the metaanalysis yielded genomewide significance for SNP on chromosome 9p (CDKN2BAS; rs6475606; P=3.6×10(-8)) and provided further evidence to support the previously reported association of IA with SNP in SOX17 on chromosome 8q (rs1072737; P=8.7×10(-5)). 22961961 2012
CUI: C0007766
Disease: Intracranial Aneurysm
Intracranial Aneurysm
0.040 GeneticVariation disease BEFREE We investigated the association between SOX17 gene polymorphisms and IA in a homogeneous Korean population. 29191544 2018
Idiopathic pulmonary arterial hypertension
0.040 GeneticVariation disease BEFREE In the past 6 years, additional pathways involved in PAH susceptibility have been described through the identification of deleterious genetic variants in potassium channels (KCNK3 and ABCC8) and transcription factors (TBX4 and SOX17), among others. 31406341 2020
Idiopathic pulmonary arterial hypertension
0.040 GeneticVariation disease BEFREE Impairment of SOX17 function might be more common in pulmonary arterial hypertension than suggested by rare mutations in SOX17. 30527956 2019
Idiopathic pulmonary arterial hypertension
0.040 GeneticVariation disease BEFREE We demonstrate familial segregation of mutations in SOX17 and AQP1 with PAH. 29650961 2018
Congenital arteriovenous malformation
0.020 GeneticVariation disease BEFREE In the American cohort, genotyped SNPs near SOX-17 (OR 0.74; 95% CI 0.56-0.98), RBBP8 (OR 0.76; 95% CI 0.62-0.94) and an imputed SNP near CDKN2B-AS1 (OR 0.79; 95% CI 0.64-0.98) were significantly associated with AVM. 25053769 2015
Associated Pulmonary Arterial Hypertension
0.020 GeneticVariation disease BEFREE Rare variants in SOX17 are associated with pulmonary arterial hypertension with congenital heart disease. 30029678 2018
CUI: C0014145
Disease: Yolk Sac Tumor
Yolk Sac Tumor
0.010 GeneticVariation disease BEFREE Many significant genes that mapped to these regions had previously been associated with specific histologies, such as EOMES (chr3) and BMP2 (chr20) in YST and SPRY2 (chr13) and SOX17 (chr8) in seminomas. 17943972 2008
CUI: C0023520
Disease: Leukodystrophy
Leukodystrophy
0.010 GeneticVariation disease BEFREE Relevance of SOX17 variants for hypomyelinating leukodystrophies and congenital anomalies of the kidney and urinary tract (CAKUT). 22348788 2012
CUI: C0149782
Disease: Squamous cell carcinoma of lung
Squamous cell carcinoma of lung
0.010 GeneticVariation disease BEFREE We identified networks regulated by known cancer drivers such as GATA3 and FOXA1 (breast cancer), SOX17 and FOXA2 (endometrial cancer), and NFE2L2, SOX2, and TP63 (squamous cell lung cancer). 25994056 2015
CUI: C0152021
Disease: Congenital heart disease
Congenital heart disease
0.010 GeneticVariation group BEFREE Rare variants in SOX17 are associated with pulmonary arterial hypertension with congenital heart disease. 30029678 2018
CUI: C0333245
Disease: Massive edema
Massive edema
0.010 GeneticVariation phenotype BEFREE In adulthood, Sox7, Sox17, and Sox18 act in a largely redundant manner to maintain blood vessel function, as adult onset vascular endothelial-specific deletion of all three SoxF genes leads to massive edema despite nearly normal vascular architecture. 26630461 2015
CUI: C1968949
Disease: Cakut
Cakut
0.010 GeneticVariation disease BEFREE Relevance of SOX17 variants for hypomyelinating leukodystrophies and congenital anomalies of the kidney and urinary tract (CAKUT). 22348788 2012
CUI: C2973725
Disease: Pulmonary arterial hypertension
Pulmonary arterial hypertension
0.010 GeneticVariation disease BEFREE Impairment of SOX17 function might be more common in pulmonary arterial hypertension than suggested by rare mutations in SOX17. 30527956 2019
CUI: C3150927
Disease: VESICOURETERAL REFLUX 3
VESICOURETERAL REFLUX 3
0.600 Biomarker disease GENOMICS_ENGLAND Mutations in SOX17 are associated with congenital anomalies of the kidney and the urinary tract. 20960469 2010
CUI: C3150927
Disease: VESICOURETERAL REFLUX 3
VESICOURETERAL REFLUX 3
0.600 Biomarker disease GENOMICS_ENGLAND Mutations in SOX17 are associated with congenital anomalies of the kidney and the urinary tract. 20960469 2010
CUI: C3150927
Disease: VESICOURETERAL REFLUX 3
VESICOURETERAL REFLUX 3
0.600 Biomarker disease GENOMICS_ENGLAND
CUI: C0042580
Disease: Vesico-Ureteral Reflux
Vesico-Ureteral Reflux
0.410 Biomarker disease CTD_human
CUI: C0042580
Disease: Vesico-Ureteral Reflux
Vesico-Ureteral Reflux
0.410 Biomarker disease HPO
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.320 Biomarker disease BEFREE SRY-box containing gene 17 (SOX17) was reported to be indispensable for embryonic development and a candidate tumor suppressor gene which antagonizes the canonical WNT/β-catenin signaling pathway in colorectal cancer. 20716954 2011
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.320 Biomarker disease CTD_human Together, our studies suggest that SOX17 is a negative modulator of canonical Wnt signaling, and that SOX17 silencing due to promoter hypermethylation is an early event during tumorigenesis and may contribute to aberrant activation of Wnt signaling in CRC. 18413743 2008