Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3160814
Disease: Cannabis use
Cannabis use
0.310 Biomarker disease BEFREE Genes such as ELTD1 on chromosome 1, in addition to genes on chromosomes 4 (eg, GABRA2) and 6 (eg, CNR1), may be associated with the genetic risk for cannabis use disorders. 18519829 2008
CUI: C3160814
Disease: Cannabis use
Cannabis use
0.310 Biomarker disease PSYGENET Genes such as ELTD1 on chromosome 1, in addition to genes on chromosomes 4 (eg, GABRA2) and 6 (eg, CNR1), may be associated with the genetic risk for cannabis use disorders. 18519829 2008
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
0.220 Biomarker disease BEFREE For example, ELTD1, a functionally validated glioblastoma oncogene located on 1p, was overexpressed. 29890994 2018
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
0.220 Biomarker disease BEFREE MicroRNA-139-5p acts as a tumor suppressor by targeting ELTD1 and regulating cell cycle in glioblastoma multiforme. 26449464 2015
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
0.220 ModifyingMutation disease RGD ELTD1, a potential new biomarker for gliomas. 23096411 2013
CUI: C0278878
Disease: Adult Glioblastoma
Adult Glioblastoma
0.210 Biomarker disease BEFREE For example, ELTD1, a functionally validated glioblastoma oncogene located on 1p, was overexpressed. 29890994 2018
CUI: C0278878
Disease: Adult Glioblastoma
Adult Glioblastoma
0.210 ModifyingMutation disease RGD ELTD1, a potential new biomarker for gliomas. 23096411 2013
CUI: C1514422
Disease: Glioblastoma, IDH-Wildtype
Glioblastoma, IDH-Wildtype
0.200 ModifyingMutation disease RGD ELTD1, a potential new biomarker for gliomas. 23096411 2013
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.100 GeneticVariation phenotype GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.100 GeneticVariation phenotype GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.100 GeneticVariation phenotype GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
Red cell distribution width determination
0.100 GeneticVariation phenotype GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
RDW - Red blood cell distribution width result
0.100 GeneticVariation phenotype GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.050 Biomarker group BEFREE Adhesion G Protein-Coupled Receptor L4 (ADGRL4/ELTD1) is an endothelial cell adhesion G protein-coupled receptor (aGPCR) which regulates physiological and tumour angiogenesis, providing an attractive target for anti-cancer therapeutics. 31775252 2019
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.050 Biomarker group BEFREE <b><i>Conclusion</i>:</b> The results of this study indicated that ELTD1 regulation of HCC progression is CAF-dependent, suggesting that ELTD1 function is regulated by its tumor microenvironment. 30026838 2018
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.050 AlteredExpression group BEFREE Untreated GL261 or G55 tumors were found to have significantly higher ELTD1 levels (IHC) compared with contralateral normal brain. 27416955 2017
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.050 Biomarker group BEFREE Importantly, ELTD1 silencing impairs endothelial sprouting and vessel formation in vitro and in vivo, drastically reducing tumor growth and greatly improving survival. 23871637 2013
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.050 AlteredExpression group BEFREE Significantly high (P < .001) in vivo levels of ELTD1 were additionally found in F98 tumors compared with normal brain tissue. 23096411 2013
CUI: C0017638
Disease: Glioma
Glioma
0.030 Biomarker disease BEFREE Taken together, our data provide a plausible mechanism for ELTD1-modulated glioma progression and suggest that ELTD1 may represent a potential therapeutic target in the prevention and therapy of glioma. 31554859 2019
CUI: C0017638
Disease: Glioma
Glioma
0.030 Biomarker disease BEFREE Tumor volume and survival data in this study show that antibodies against ELTD1 inhibit glioma growth just as effectively or even more so compared with other therapeutic targets studied, including anti-VEGF antibody therapy. 27416955 2017
CUI: C0017638
Disease: Glioma
Glioma
0.030 AlteredExpression disease BEFREE Validation was done with immunohistochemistry, which was used to detect levels of ELTD1 in human high-grade gliomas and rat F98 glioma tumors. 23096411 2013
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.020 Biomarker group BEFREE The upregulation of ELTD1 ([epidermal growth factor (EGF), latrophilin and seven transmembrane domain-containing 1] on chromosome 1) in tumor cells has been reported in several types of cancer and correlates with poor cancer prognosis. 31554859 2019
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.020 Biomarker group BEFREE The upregulation of ELTD1 ([epidermal growth factor (EGF), latrophilin and seven transmembrane domain-containing 1] on chromosome 1) in tumor cells has been reported in several types of cancer and correlates with poor cancer prognosis. 31554859 2019
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.020 Biomarker group BEFREE <b><i>Results</i>:</b> Clinicopathologic correlations and <i>in vivo</i> models indicated ELTD1 as a tumor suppressor gene, whereas <i>in vitro</i> experiments suggested that ELTD1 could promote malignancy in HCC cell lines. 30026838 2018
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.020 Biomarker group BEFREE <b><i>Results</i>:</b> Clinicopathologic correlations and <i>in vivo</i> models indicated ELTD1 as a tumor suppressor gene, whereas <i>in vitro</i> experiments suggested that ELTD1 could promote malignancy in HCC cell lines. 30026838 2018