Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.100 GeneticVariation disease GWASCAT Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease. 29212778 2018
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
0.080 Biomarker phenotype BEFREE SIP1 serves a role in HBx‑induced liver cancer growth and metastasis. 31793654 2019
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
0.080 Biomarker phenotype BEFREE The elevated ARK5 expression was closely associated with cancer metastasis and patient survival, and it seemed to function in GC cells migration and invasion via EMT alteration, together with the alteration of the mTOR/p70S6k signals, Slug and SIP1, thus providing a potential therapeutic target for GC. 28662499 2017
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
0.080 AlteredExpression phenotype BEFREE TWIST1, Slug, Snail, SIP1, and NF-κB are overexpressed in various tumors and associated with metastasis and poor prognosis. 23150175 2013
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
0.080 Biomarker phenotype BEFREE It is proposed that the elevated expression of HIF-2α, TWIST2, and SIP1 can contribute to invasion and metastasis of ACC, and there might be some correlation between the hypoxia microenvironment and EMT in ACC. 22103974 2012
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
0.080 AlteredExpression phenotype BEFREE Overexpression of SIP1 and downregulation of E-cadherin predict delayed neck metastasis in stage I/II oral tongue squamous cell carcinoma after partial glossectomy. 21913013 2012
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
0.080 Biomarker phenotype BEFREE The prognostic value of SIP1 and its role in DNA damage response establish a link between genetic instability and metastasis and suggest a potential importance for this protein as a therapeutic target. 19706487 2009
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
0.080 Biomarker phenotype BEFREE Together, these microRNAs cooperatively regulate expression of the E-cadherin transcriptional repressors ZEB1 (also known as deltaEF1) and SIP1 (also known as ZEB2), factors previously implicated in EMT and tumour metastasis. 18376396 2008
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
0.080 AlteredExpression phenotype BEFREE Using reverse-transcription polymerase chain reaction, mRNA in situ hybridization, and Western blotting, we analyzed the expression and localization of the Snail, Slug, and SIP1 transcription factors and E-cadherin in 78 effusions, 41 primary carcinomas, and 15 solid metastases. 17024425 2006
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.070 AlteredExpression phenotype BEFREE Long non-coding RNA NORAD upregulate SIP1 expression to promote cell proliferation and invasion in cervical cancer. 30119219 2018
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.070 Biomarker phenotype BEFREE Mechanistic studies suggested that SIP1-mediated EMT might be responsible for TRIM37-facilitated GC cells migration and invasion. 30573971 2018
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.070 Biomarker phenotype BEFREE The elevated ARK5 expression was closely associated with cancer metastasis and patient survival, and it seemed to function in GC cells migration and invasion via EMT alteration, together with the alteration of the mTOR/p70S6k signals, Slug and SIP1, thus providing a potential therapeutic target for GC. 28662499 2017
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.070 Biomarker phenotype BEFREE It is proposed that the elevated expression of HIF-2α, TWIST2, and SIP1 can contribute to invasion and metastasis of ACC, and there might be some correlation between the hypoxia microenvironment and EMT in ACC. 22103974 2012
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.070 AlteredExpression phenotype BEFREE Multiple logistic regression analysis including clinicopathological and molecular factors revealed that overexpression of SIP1 (P = 0.005), loss of E-cadherin (P = 0.046), and vascular invasion (P = 0.024) were independently correlated with DNM. 21913013 2012
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.070 Biomarker phenotype BEFREE In the present study, we investigated the potential role of SIP1 in the regulation of vimentin during the EMT associated with breast tumor cell migration and invasion. 16568083 2006
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.070 Biomarker phenotype BEFREE Snail and SIP1 increase cancer invasion by upregulating MMP family in hepatocellular carcinoma cells. 15026811 2004
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome
0.060 GeneticVariation disease BEFREE Sip1 mutation in humans was shown to cause Mowat-Wilson syndrome, a syndromic form of Hirschprung's disease. 30266271 2019
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome
0.060 GeneticVariation disease BEFREE The Sip1 mutation plays the main role in pathogenesis of the Mowat-Wilson syndrome, which is characterized by the pronounced epileptic symptoms. 30056076 2018
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.060 Biomarker group BEFREE The elevated ARK5 expression was closely associated with cancer metastasis and patient survival, and it seemed to function in GC cells migration and invasion via EMT alteration, together with the alteration of the mTOR/p70S6k signals, Slug and SIP1, thus providing a potential therapeutic target for GC. 28662499 2017
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome
0.060 GeneticVariation disease BEFREE De novo inbred heterozygous Zeb2/Sip1 mutant mice uniquely generated by germ-line conditional knockout exhibit craniofacial, callosal and behavioral defects associated with Mowat-Wilson syndrome. 26319231 2015
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome
0.060 Biomarker disease BEFREE These findings may help to clarify the unknown roles of SIP1 in these cells and the pathoetiology of Mowat-Wilson syndrome. 24243579 2014
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.060 PosttranslationalModification group BEFREE However, most pancreatic cancers express miR-200a and miR-200b, but this expression does not affect SIP1 expression, as the SIP1 promoter is silenced by hypermethylation and in these cancers E-cadherin is generally expressed. 20551052 2010
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.060 Biomarker group BEFREE Here, we performed a comparative study of SIP1 and ZEB1 proteins in cancer cell lines and in one form of human malignancy, carcinoma of the bladder. 19706487 2009
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.060 Biomarker group BEFREE Of 95 ovarian tumors, the expression of Snail, Slug, SIP1, and Twist increased stepwise in benign, borderline, and malignant tumors. 19536615 2009
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome
0.060 Biomarker disease BEFREE The SIP1 gene associated with the Mowat-Wilson syndrome was not included in the deleted genomic region. 18812405 2009