Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.600 GeneticVariation disease UNIPROT We also found loss of heterozygosity in the lung cancer, suggesting that TSSC5 may be a conventional tumor suppressor gene in the adult human lung and an imprinted tumor suppressor gene in the fetal kidney. 9751628 1998
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.600 CausalMutation disease CLINVAR
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.600 CausalMutation disease CGI
CUI: C0024121
Disease: Lung Neoplasms
Lung Neoplasms
0.500 CausalMutation group CGI
CUI: C0024121
Disease: Lung Neoplasms
Lung Neoplasms
0.500 Biomarker group CTD_human
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.500 Biomarker disease CTD_human
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.500 CausalMutation disease CGI
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.460 Biomarker disease BEFREE Our results suggest that SLC22A18 may act as a tumor suppressor by regulating the expression levels of cell growth-related proteins, and vinca alkaloids might show therapeutic efficacy against low-SLC22A18-expressing breast cancer. 30145211 2018
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.460 AlteredExpression disease BEFREE The results of Kaplan-Meier analysis indicated that SLC22A18 expression was associated with relapse-free survival (RFS) of breast cancer. 21144813 2011
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.460 Biomarker disease BEFREE Gain of imprinting of SLC22A18 sense and antisense transcripts in human breast cancer. 16624517 2006
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.460 AlteredExpression disease BEFREE HET/SAF-B protein and mRNA were detected at varying levels in all of the eight breast cancer cell lines examined. 10999774 2000
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.460 GeneticVariation disease BEFREE Because this region frequently is altered in neoplasms and in the genetic disease Beckwith-Wiedemann syndrome, we carried out a mutational analysis in tumor cell lines and Beckwith-Wiedemann syndrome samples that resulted in the identification of genetic alterations in the BWR1A gene: an insertion that introduced a stop codon in the breast cancer cell line BT549 and a point mutation in the rhabdomyosarcoma cell line TE125-T. 9520460 1998
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.460 Biomarker disease BEFREE We were able to show that HET is localized in the nuclear matrix in various breast cancer cell lines. 9328833 1997
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.460 Biomarker disease CTD_human
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.460 Biomarker disease HPO
CUI: C0206656
Disease: Embryonal Rhabdomyosarcoma
Embryonal Rhabdomyosarcoma
0.400 GeneticVariation disease ORPHANET Transcriptional map of 170-kb region at chromosome 11p15.5: identification and mutational analysis of the BWR1A gene reveals the presence of mutations in tumor samples. 9520460 1998
CUI: C0206656
Disease: Embryonal Rhabdomyosarcoma
Embryonal Rhabdomyosarcoma
0.400 Biomarker disease HPO
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.360 Biomarker disease BEFREE Our results suggest that SLC22A18 may act as a tumor suppressor by regulating the expression levels of cell growth-related proteins, and vinca alkaloids might show therapeutic efficacy against low-SLC22A18-expressing breast cancer. 30145211 2018
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.360 AlteredExpression disease BEFREE The results of Kaplan-Meier analysis indicated that SLC22A18 expression was associated with relapse-free survival (RFS) of breast cancer. 21144813 2011
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.360 Biomarker disease BEFREE Gain of imprinting of SLC22A18 sense and antisense transcripts in human breast cancer. 16624517 2006
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.360 AlteredExpression disease BEFREE HET/SAF-B protein and mRNA were detected at varying levels in all of the eight breast cancer cell lines examined. 10999774 2000
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.360 GeneticVariation disease BEFREE Because this region frequently is altered in neoplasms and in the genetic disease Beckwith-Wiedemann syndrome, we carried out a mutational analysis in tumor cell lines and Beckwith-Wiedemann syndrome samples that resulted in the identification of genetic alterations in the BWR1A gene: an insertion that introduced a stop codon in the breast cancer cell line BT549 and a point mutation in the rhabdomyosarcoma cell line TE125-T. 9520460 1998
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.360 Biomarker disease BEFREE We were able to show that HET is localized in the nuclear matrix in various breast cancer cell lines. 9328833 1997
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.360 Biomarker disease CTD_human
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.320 AlteredExpression group BEFREE SPECIMENS AND METHODS: Immunohistochemistry was used to examine SLC22A18 protein expression in the breast tumors. 21144813 2011