Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4313
Gene Symbol: MMP2
MMP2
CUI: C1850155
Disease: TORG-WINCHESTER SYNDROME
TORG-WINCHESTER SYNDROME
0.790 GeneticVariation BEFREE A novel mutation in the matrix metallopeptidase 2 coding gene associated with intrafamilial variability of multicentric osteolysis, nodulosis, and arthropathy. 31268248

2019

Entrez Id: 4313
Gene Symbol: MMP2
MMP2
CUI: C1850155
Disease: TORG-WINCHESTER SYNDROME
TORG-WINCHESTER SYNDROME
0.790 Biomarker BEFREE We characterize the clinical, radiographic and molecular findings in all individuals with molecularly proven MONA from the present cohort and previous reports, and provide a comprehensive review of the MMP2 related disorders. 26601801

2016

Entrez Id: 4313
Gene Symbol: MMP2
MMP2
CUI: C1850155
Disease: TORG-WINCHESTER SYNDROME
TORG-WINCHESTER SYNDROME
0.790 GeneticVariation BEFREE Here, we describe the molecular and functional analysis of a novel MMP2 mutation in two adult Italian siblings with MONA. 25273674

2014

Entrez Id: 4313
Gene Symbol: MMP2
MMP2
CUI: C1850155
Disease: TORG-WINCHESTER SYNDROME
TORG-WINCHESTER SYNDROME
0.790 GeneticVariation BEFREE Torg syndrome is caused by homozygous or compound heterozygous mutations in the matrix metalloproteinase 2 (MMP2) gene. 24637309

2014

Entrez Id: 4313
Gene Symbol: MMP2
MMP2
CUI: C1850155
Disease: TORG-WINCHESTER SYNDROME
TORG-WINCHESTER SYNDROME
0.790 GeneticVariation BEFREE MMP2 gene sequence analysis excluded multicentric osteolysis, nodulosis and arthropathy. 20560960

2010

Entrez Id: 4313
Gene Symbol: MMP2
MMP2
CUI: C1850155
Disease: TORG-WINCHESTER SYNDROME
TORG-WINCHESTER SYNDROME
0.790 GeneticVariation BEFREE A novel homozygous MMP2 mutation in a patient with Torg-Winchester syndrome. 20720557

2010

Entrez Id: 4313
Gene Symbol: MMP2
MMP2
CUI: C1850155
Disease: TORG-WINCHESTER SYNDROME
TORG-WINCHESTER SYNDROME
0.790 GeneticVariation BEFREE The two well-described osteolysis syndromes associated with matrix metalloproteinase-2 deficiency and mutations in the metalloproteinase-2 gene are Torg-Winchester syndrome and nodulosis-arthropathy-osteolysis variant. 19653001

2010

Entrez Id: 4313
Gene Symbol: MMP2
MMP2
CUI: C1850155
Disease: TORG-WINCHESTER SYNDROME
TORG-WINCHESTER SYNDROME
0.790 GeneticVariation BEFREE We sequenced the MMP2 gene in a patient with clinical and radiographic findings of Torg syndrome. 17059372

2007

Entrez Id: 4313
Gene Symbol: MMP2
MMP2
CUI: C1850155
Disease: TORG-WINCHESTER SYNDROME
TORG-WINCHESTER SYNDROME
0.790 GeneticVariation BEFREE We questioned whether sporadic idiopathic multicentric osteolysis with nephropathy is allelic with nodulosis-arthropathy osteolysis syndrome and undertook sequence analysis of the matrix metalloproteinase 2 gene in three unrelated affected boys. 17563705

2007

Entrez Id: 4313
Gene Symbol: MMP2
MMP2
CUI: C1850155
Disease: TORG-WINCHESTER SYNDROME
TORG-WINCHESTER SYNDROME
0.790 GeneticVariation UNIPROT A novel homozygous MMP2 mutation in a family with Winchester syndrome. 16542393

2006

Entrez Id: 4313
Gene Symbol: MMP2
MMP2
CUI: C1850155
Disease: TORG-WINCHESTER SYNDROME
TORG-WINCHESTER SYNDROME
0.790 GeneticVariation UNIPROT Winchester syndrome caused by a homozygous mutation affecting the active site of matrix metalloproteinase 2. 15691365

2005

Entrez Id: 4313
Gene Symbol: MMP2
MMP2
CUI: C1850155
Disease: TORG-WINCHESTER SYNDROME
TORG-WINCHESTER SYNDROME
0.790 GeneticVariation UNIPROT Mutation of the matrix metalloproteinase 2 gene (MMP2) causes a multicentric osteolysis and arthritis syndrome. 11431697

2001

Entrez Id: 4313
Gene Symbol: MMP2
MMP2
CUI: C1850155
Disease: TORG-WINCHESTER SYNDROME
TORG-WINCHESTER SYNDROME
0.790 Biomarker CTD_human

Entrez Id: 4313
Gene Symbol: MMP2
MMP2
CUI: C1850155
Disease: TORG-WINCHESTER SYNDROME
TORG-WINCHESTER SYNDROME
0.790 CausalMutation CLINVAR

Entrez Id: 4313
Gene Symbol: MMP2
MMP2
CUI: C1850155
Disease: TORG-WINCHESTER SYNDROME
TORG-WINCHESTER SYNDROME
0.790 Biomarker GENOMICS_ENGLAND

Entrez Id: 4313
Gene Symbol: MMP2
MMP2
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 AlteredExpression BEFREE JMJD2D was required for expression of β-catenin in CRC cell lines; ectopic expression of JMJD2D increased the promoter activities of genes regulated by β-catenin (MYC, CCND1, MMP2, and MMP9). 30472235

2019

Entrez Id: 4313
Gene Symbol: MMP2
MMP2
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 Biomarker BEFREE In an analysis of the miRNA target genes, we found that CDH2, KNG1, and MMP2 were correlated with CRC metastasis. 30807603

2019

Entrez Id: 4313
Gene Symbol: MMP2
MMP2
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 AlteredExpression BEFREE The present study therefore investigated whether aortic MMP-2 activity is increased by oxidative stress in early hypertension and then contributes to hypertrophic arterial remodeling by reducing the levels of calponin-1. 30339939

2019

Entrez Id: 4313
Gene Symbol: MMP2
MMP2
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 AlteredExpression BEFREE Vascular MMP-2 expression and activity were assessed by gel zymography, Western blot, and in situ zymography increased with hypertension. 30399409

2019

Entrez Id: 4313
Gene Symbol: MMP2
MMP2
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 GeneticVariation BEFREE The associations of urinary cadmium with hypertension risk were modified by rs14070 (P-value for interaction = 0.022) and rs7201 (P-value for interaction = 0.009) in gene MMP-2. 30684802

2019

Entrez Id: 4313
Gene Symbol: MMP2
MMP2
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 Biomarker BEFREE The expressions of VEGF and MMP-2 in serum of CRC patients were correlated with the depth of tumor infiltration, Dukes' staging, CLM and lymph node metastasis (p<0.05). 29917190

2018

Entrez Id: 4313
Gene Symbol: MMP2
MMP2
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 AlteredExpression BEFREE Twist1/2 activates MMP2 expression via binding to its promoter in colorectal cancer. 30556860

2018

Entrez Id: 4313
Gene Symbol: MMP2
MMP2
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 Biomarker BEFREE Our findings in this study provide understanding of MMP2 regulation in CRC and may also shed lights on the development of anti-CRC treatments. 29260353

2018

Entrez Id: 4313
Gene Symbol: MMP2
MMP2
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 AlteredExpression BEFREE Tumor and adjacent healthy tissues were obtained from 100 patients diagnosed with CRC. miR-466 expression was determined by quantitative reverse transcription polymerase chain reaction (qRT-PCR). mRNA and protein levels of cyclin D1, apoptosis regulator BAX (BAX), and matrix metalloproteinase-2 (MMP-2) were analyzed by qRT-PCR and Western blot, respectively, in SW-620 CRC cells transfected with miR-466 mimics or negative control miRNA. 29338680

2018

Entrez Id: 4313
Gene Symbol: MMP2
MMP2
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 AlteredExpression BEFREE This resulted in the increased expression of matrix metalloproteinase 2 (MMP2), matrix metalloproteinase 9 (MMP9) and vascular endothelial growth factor (VEGF), and the subsequent promotion of CRC cell invasion. 30228782

2018