TIMP2, TIMP metallopeptidase inhibitor 2, 7077

N. diseases: 404; N. variants: 20
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3744787
rs3744787
Entrez Id: 7077;100653515
Gene Symbol: TIMP2;CEP295NL
TIMP2;CEP295NL
CUI: C0035242
Disease:
Respiratory Tract Diseases
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs9905388
rs9905388
Entrez Id: 7077
Gene Symbol: TIMP2
TIMP2
CUI: C0205682
Disease:
Waist-Hip Ratio
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1973232
rs1973232
Entrez Id: 7077
Gene Symbol: TIMP2
TIMP2
CUI: C4317009
Disease:
Diverticular Diseases
A 0.700 GeneticVariation GWASCAT Genome-wide association analyses identify 39 new susceptibility loci for diverticular disease. 30177863 2018
dbSNP: rs2376999
rs2376999
Entrez Id: 7077;100653515
Gene Symbol: TIMP2;CEP295NL
TIMP2;CEP295NL
CUI: C2985280
Disease:
Blood Protein Measurement
A 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
dbSNP: rs3744790
rs3744790
Entrez Id: 7077;100653515
Gene Symbol: TIMP2;CEP295NL
TIMP2;CEP295NL
CUI: C0341106
Disease:
Eosinophilic esophagitis
0.700 GeneticVariation GWASCAT Genome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease. 25017104 2014
dbSNP: rs4789939
rs4789939
Entrez Id: 7077;100653515
Gene Symbol: TIMP2;CEP295NL
TIMP2;CEP295NL
CUI: C0013312
Disease:
Dupuytren Contracture
0.700 GeneticVariation GWASCAT Wnt signaling and Dupuytren's disease. 21732829 2011
dbSNP: rs4789939
rs4789939
Entrez Id: 7077;100653515
Gene Symbol: TIMP2;CEP295NL
TIMP2;CEP295NL
CUI: C4082974
Disease:
Dupuytren's Disease
0.700 GeneticVariation GWASDB Wnt signaling and Dupuytren's disease. 21732829 2011
dbSNP: rs4789937
rs4789937
Entrez Id: 7077;100653515
Gene Symbol: TIMP2;CEP295NL
TIMP2;CEP295NL
CUI: C2700366
Disease:
Adiponectin Measurement
0.700 GeneticVariation GWASDB Adiponectin concentrations: a genome-wide association study. 20887962 2010
dbSNP: rs11658743
rs11658743
Entrez Id: 7077;100653515
Gene Symbol: TIMP2;CEP295NL
TIMP2;CEP295NL
CUI: C0595995
Disease:
Idiopathic scoliosis
0.010 GeneticVariation BEFREE The remaining two polymorphisms (rs2377005, rs11658743) showed no association with either clinical or radiographic IS characteristics. 31119800 2019
dbSNP: rs2277698
rs2277698
Entrez Id: 7077;100653515
Gene Symbol: TIMP2;CEP295NL
TIMP2;CEP295NL
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.010 GeneticVariation BEFREE Our study indicated that TIMP-2 rs2277698 was associated with breast cancer susceptibility. 31088428 2019
dbSNP: rs2277698
rs2277698
Entrez Id: 7077;100653515
Gene Symbol: TIMP2;CEP295NL
TIMP2;CEP295NL
CUI: C0085215
Disease:
Ovarian Failure, Premature
0.010 GeneticVariation BEFREE The TIMP2G > C (rs8179090) and G > A (rs2277698) alleles were strongly associated with POI. 30583769 2019
dbSNP: rs2277698
rs2277698
Entrez Id: 7077;100653515
Gene Symbol: TIMP2;CEP295NL
TIMP2;CEP295NL
CUI: C0025322
Disease:
Premature Menopause
0.010 GeneticVariation BEFREE The aim of our study was to investigate whether the TIMP polymorphisms TIMP1T > C (rs4898), TIMP1G > A (rs6609533), TIMP2G > C (rs8179090), TIMP2G > A (rs2277698), TIMP3G > A (rs135029), and TIMP4T > C (rs3755724), which regulate matrix metalloproteinases (MMPs), confer a risk for primary ovarian insufficiency (POI) in Korean women (further studies would be required to evaluate the associations between TIMP polymorphisms and POI in other populations). 30583769 2019
dbSNP: rs2277698
rs2277698
Entrez Id: 7077;100653515
Gene Symbol: TIMP2;CEP295NL
TIMP2;CEP295NL
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE Our study indicated that TIMP-2 rs2277698 was associated with breast cancer susceptibility. 31088428 2019
dbSNP: rs2277700
rs2277700
Entrez Id: 7077
Gene Symbol: TIMP2
TIMP2
CUI: C0595995
Disease:
Idiopathic scoliosis
0.010 GeneticVariation BEFREE We identified four TIMP2 polymorphisms (rs11077401, rs2376999, rs2277700, and rs4789934) that were associated with a higher risk of the progressive IS form. 31119800 2019
dbSNP: rs2377005
rs2377005
Entrez Id: 7077;100653515
Gene Symbol: TIMP2;CEP295NL
TIMP2;CEP295NL
CUI: C0595995
Disease:
Idiopathic scoliosis
0.010 GeneticVariation BEFREE The remaining two polymorphisms (rs2377005, rs11658743) showed no association with either clinical or radiographic IS characteristics. 31119800 2019
dbSNP: rs4789934
rs4789934
Entrez Id: 7077
Gene Symbol: TIMP2
TIMP2
CUI: C0595995
Disease:
Idiopathic scoliosis
0.010 GeneticVariation BEFREE We identified four TIMP2 polymorphisms (rs11077401, rs2376999, rs2277700, and rs4789934) that were associated with a higher risk of the progressive IS form. 31119800 2019
dbSNP: rs4789936
rs4789936
Entrez Id: 7077;100653515
Gene Symbol: TIMP2;CEP295NL
TIMP2;CEP295NL
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE Bioinformatics analysis found that rs4789936 was likely to affect transcription factor binding, motifs, DNase footprint, and DNase peaks; and TIMP-2 was under-expressed in breast cancer, the risk allele of rs4789936 was associated with increased expression of TIMP-2 in peripheral blood samples. 31088428 2019
dbSNP: rs4789936
rs4789936
Entrez Id: 7077;100653515
Gene Symbol: TIMP2;CEP295NL
TIMP2;CEP295NL
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.010 GeneticVariation BEFREE Bioinformatics analysis found that rs4789936 was likely to affect transcription factor binding, motifs, DNase footprint, and DNase peaks; and TIMP-2 was under-expressed in breast cancer, the risk allele of rs4789936 was associated with increased expression of TIMP-2 in peripheral blood samples. 31088428 2019
dbSNP: rs540397728
rs540397728
Entrez Id: 7077;100653515
Gene Symbol: TIMP2;CEP295NL
TIMP2;CEP295NL
CUI: C0036341
Disease:
Schizophrenia
0.010 GeneticVariation BEFREE WES based screening of an independent SZ cohort (n = 370) identified 4 additional rare missense variants (p.Leu20Met, p.Ala26Ser, p.Lys48Arg and p. Ile217Leu) and a splice variant rs540397728 (NM_003255:c.232-5T>C), also predicted to be damaging, increasing the likelihood of contribution of this gene to SZ risk. 29385606 2019
dbSNP: rs578083142
rs578083142
Entrez Id: 7077
Gene Symbol: TIMP2
TIMP2
CUI: C0036341
Disease:
Schizophrenia
0.010 GeneticVariation BEFREE WES based screening of an independent SZ cohort (n = 370) identified 4 additional rare missense variants (p.Leu20Met, p.Ala26Ser, p.Lys48Arg and p. Ile217Leu) and a splice variant rs540397728 (NM_003255:c.232-5T>C), also predicted to be damaging, increasing the likelihood of contribution of this gene to SZ risk. 29385606 2019
dbSNP: rs8179090
rs8179090
Entrez Id: 7077
Gene Symbol: TIMP2
TIMP2
CUI: C0595995
Disease:
Idiopathic scoliosis
0.010 GeneticVariation BEFREE The influence of the G allele of the rs8179090 on the clinical course of IS has not yet been confirmed. 31119800 2019
dbSNP: rs8179090
rs8179090
Entrez Id: 7077
Gene Symbol: TIMP2
TIMP2
CUI: C0085215
Disease:
Ovarian Failure, Premature
0.010 GeneticVariation BEFREE The TIMP2G > C (rs8179090) and G > A (rs2277698) alleles were strongly associated with POI. 30583769 2019
dbSNP: rs8179090
rs8179090
Entrez Id: 7077
Gene Symbol: TIMP2
TIMP2
CUI: C0025322
Disease:
Premature Menopause
0.010 GeneticVariation BEFREE The aim of our study was to investigate whether the TIMP polymorphisms TIMP1T > C (rs4898), TIMP1G > A (rs6609533), TIMP2G > C (rs8179090), TIMP2G > A (rs2277698), TIMP3G > A (rs135029), and TIMP4T > C (rs3755724), which regulate matrix metalloproteinases (MMPs), confer a risk for primary ovarian insufficiency (POI) in Korean women (further studies would be required to evaluate the associations between TIMP polymorphisms and POI in other populations). 30583769 2019
dbSNP: rs2277698
rs2277698
Entrez Id: 7077;100653515
Gene Symbol: TIMP2;CEP295NL
TIMP2;CEP295NL
CUI: C0752156
Disease:
Dural Arteriovenous Fistula
0.010 GeneticVariation BEFREE There was a weak difference in associations of tissue inhibitor of metalloproteinase (TIMP)-2 (rs2277698) gene polymorphism and DAVF patients subgrouped by CVR grading. 29431912 2018
dbSNP: rs4789936
rs4789936
Entrez Id: 7077;100653515
Gene Symbol: TIMP2;CEP295NL
TIMP2;CEP295NL
CUI: C0038454
Disease:
Cerebrovascular accident
0.010 GeneticVariation BEFREE We observed the rs4789936 had a decreased risk of LAA stroke according to the codominant (OR = 0.64, 95% CI = 0.44-0.92, <i>P</i> = 0.026), dominant (OR = 0.62, 95% CI = 0.43-0.88, <i>P</i> = 0.008), overdominant (OR = 0.68, 95% CI = 0.48-0.98, <i>P</i> = 0.039), log-additive (OR = 0.68, 95% CI = 0.51-0.91, <i>P</i> = 0.009) models analyses. 29435135 2018