REL, REL proto-oncogene, NF-kB subunit, 5966

N. diseases: 90; N. variants: 5
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease
0.550 Biomarker disease CTD_human A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3). 21037568 2010
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease
0.550 Biomarker disease BEFREE In addition, c-rel has been activated by a retroviral promoter insertion in an avian B-cell lymphoma, and amplifications of REL (human c-rel) are frequently seen in Hodgkin's lymphomas and diffuse large B-cell lymphomas, and in some follicular and mediastinal B-cell lymphomas. 14755244 2004
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease
0.550 AlteredExpression disease LHGDN Our results demonstrate that there is differential c-REL protein expression in cHL in comparison with NLPHL and suggest that c-REL may play a role in the pathogenesis of classic Hodgkin lymphoma. 15551733 2004
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease
0.550 Biomarker disease BEFREE Hodgkin's lymphoma cell lines are characterized by frequent aberrations on chromosomes 2p and 9p including REL and JAK2. 12478664 2003
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease
0.550 AlteredExpression disease LHGDN Our data confirm previous cytogenetic results from primary Hodgkin's tumors suggesting an important pathogenic role of REL and JAK2 in this disease. 12478664 2003
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease
0.550 GeneticVariation disease LHGDN Recurrent involvement of the REL and BCL11A loci in classical Hodgkin lymphoma. 11830502 2002
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease
0.550 Biomarker disease BEFREE BCL11A coamplified with REL in B-NHL cases and HD lymphoma cell lines with gains and amplifications of 2p13, suggesting that BCL11A may be involved in lymphoid malignancies through either chromosomal translocation or amplification. 11719382 2001
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease
0.550 GenomicAlterations disease CGI