Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.010 Biomarker disease BEFREE The restricted V(H) gene usage in anticolon autoantibodies producing B-cell clones suggests that a particular antigenic stimulus contributes to the pathogenesis of UC. 11438490 2001
CUI: C1336753
Disease: Thyroid Lymphoma
Thyroid Lymphoma
0.010 PosttranslationalModification disease BEFREE DNA sequence of immunoglobulin heavy chain variable region gene in thyroid lymphoma. 11676854 2001
CUI: C0038273
Disease: Stereotypic Movement Disorder
Stereotypic Movement Disorder
0.010 Biomarker phenotype BEFREE Immunoglobulin heavy chain variable region gene repertoire and B-cell receptor stereotypes in Indian patients with chronic lymphocytic leukemia. 26942309 2016
CUI: C1336077
Disease: Sporadic Burkitt's lymphoma
Sporadic Burkitt's lymphoma
0.010 GeneticVariation disease BEFREE However the level of somatic mutation and the effect of antigen selection on V(H) gene were diverse in these three cases, and the relationship between V(H) gene somatic mutation status and intraclonal diversity was unclear in sBL. 11908722 2002
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.040 Biomarker disease BEFREE Biased usage of synovial immunoglobulin heavy chain variable region 4 by the anti-glucose-6-phosphate isomerase antibody in patients with rheumatoid arthritis. 17611644 2007
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.040 GeneticVariation disease BEFREE A relationship between these secondary V(H) gene rearrangements and the autoimmunity characteristic of RA should be considered. 11034605 2000
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.040 GeneticVariation disease BEFREE Sequence analysis of immunoglobulin heavy-chain variable region genes from the synovium of a rheumatoid arthritis patient shows little evidence of mutation but diverse CDR3. 7751018 1995
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.040 GeneticVariation disease BEFREE To investigate the contribution of polymorphism in the immunoglobulin heavy chain variable region V1-69 gene set to genetic susceptibility to rheumatoid arthritis (RA) in Czech and British patients. 11961170 2002
CUI: C1709781
Disease: Pyothorax-Associated Lymphoma
Pyothorax-Associated Lymphoma
0.010 PosttranslationalModification disease BEFREE DNA sequences of the immunoglobulin heavy chain variable region gene in pyothorax-associated lymphoma. 12065872 2002
CUI: C0033845
Disease: Pseudotumor Cerebri
Pseudotumor Cerebri
0.010 Biomarker disease BEFREE To investigate the hypothesis that pseudotumor cerebri (PTC) is associated with humoral immunity, we analyzed immunoglobulin heavy chain variable region (Ig-VH) genes of B cells in the cerebrospinal fluid (CSF) of 10 patients with PTC. 15622452 2004
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 GeneticVariation group BEFREE Importantly, we confirmed by multivariate analysis that this was independent of IgHV mutational status or subset #2 stereotyped receptor (<i>P</i> < 0.0001).<b>Conclusions:</b> We have demonstrated for the first time that a light chain can affect CLL prognosis and that IgLV3-21 light chain usage defines a new subgroup of CLL patients with poor prognosis.<i>Clin Cancer Res; 24(20); 5048-57.©2018 AACR</i>. 29945996 2018
Precursor B-cell lymphoblastic leukemia
0.020 GeneticVariation disease BEFREE The lack of mutation in VH gene sequences suggests that SM may differ between PB-LBL and B-ALL. 11710683 2001
Precursor B-cell lymphoblastic leukemia
0.020 Biomarker disease BEFREE The aim of this study was to investigate whether immunoglobulin heavy chain FR-derived peptides shared in each IgHV family are potential CTL epitopes presented by B-cell acute lymphoblastic leukemia (B-ALL). 17517179 2007
CUI: C0032131
Disease: Plasmacytoma
Plasmacytoma
0.010 Biomarker disease BEFREE Sequences required for the function of the mouse V1 immunoglobulin heavy chain variable-region (VH) promoter were identified by transient transfection of the normal and mutated promoters into plasmacytoma cells. 3118372 1987
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma
0.010 Biomarker disease BEFREE To investigate the hypothesis that pseudotumor cerebri (PTC) is associated with humoral immunity, we analyzed immunoglobulin heavy chain variable region (Ig-VH) genes of B cells in the cerebrospinal fluid (CSF) of 10 patients with PTC. 15622452 2004
Pancreatitis due to pancreatic duct obstruction
0.010 Biomarker disease BEFREE However, the rate of unmutated VH fragments in type 1 AIP (17%) was higher than that in obstructive pancreatitis (5.1%) (P= 0.010). 22524659 2012
Ocular Adnexal Mucosa-Associated Lymphoid Tissue Lymphoma
0.010 Biomarker disease BEFREE Sequence analysis of VH genes showed that an autoimmune mechanism may be involved in the lymphomagenesis of ocular adnexal MALT lymphoma. 11454995 2001
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.050 Biomarker group BEFREE The tumor immunoglobulin heavy chain variable region was more frequently unmutated in CLL cells of LR patients, and the mevalonate pathway, which generates Vγ9Vδ2 TCR ligands, was more active in unmutated CLL cells. 22932792 2012
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.050 Biomarker group BEFREE Immunoglobulin heavy chain variable region family usage is independent of tumor cell phenotype in human B lineage leukemias. 1700749 1990
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.050 GeneticVariation group BEFREE The immunoglobulins secreted by these cell lines reacted variably with a panel of anti-idiotypic antibodies, indicating that the tumor was heterogeneous; however, one antibody, 4D6, reacted strongly with the product of all the heterohybridomas. cDNA for the immunoglobulin heavy chain variable-region genes expressed in these heterohybridomas was cloned and sequenced. 3496601 1987
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.050 GeneticVariation group BEFREE We have previously shown that the cytogenetic breakpoints of one t(14;14)(q11;q32) chromosome and two inv(14)(q11;q32) chromosomes in T-cell tumors from AT and non-AT patients join the T-cell receptor alpha chain locus, at chromosome band 14q11, with a region(s) at 14q32 centromeric of the immunoglobulin heavy chain variable region (VH) gene IGHV. 3194418 1988
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.050 Biomarker group BEFREE In the other two patients, a similar VH band pattern was observed and also was compared using direct sequencing, which demonstrated sequence differences between tumors from the two sites. 15372481 2004
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.030 GeneticVariation disease BEFREE Susceptibility to multiple sclerosis is associated with the proximal immunoglobulin heavy chain variable region. 1672695 1991
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.030 Biomarker disease BEFREE Susceptibility to multiple sclerosis and the immunoglobulin heavy chain variable region. 8568530 1995
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.030 GeneticVariation disease BEFREE Immunoglobulin heavy chain variable region polymorphisms and multiple sclerosis susceptibility. 8496340 1993