Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 30968
Gene Symbol: STOML2
STOML2
0.040 GeneticVariation disease BEFREE Our results serve as an explanation for the exclusive autoimmunogenicity of the hyperphosphorylated variant of P-7 and for the different hazard ratios of pP-7 carriers from different ethnic origins to develop MGUS/MM/WM. 25677163 2015
Entrez Id: 30968
Gene Symbol: STOML2
STOML2
0.040 Biomarker disease BEFREE In conclusion, the mechanisms responsible for the defective dephosphorylation and maintaining the hyperphosphorylated state of P-7 and other autoantigenic paraprotein targets have been elucidated, facilitating the identification of the genetic basis underlying this phenomenon which is obviously common in the pathogenesis of MGUS/MM/WM and not restricted to pP-7 cases. 24676687 2014
Entrez Id: 30968
Gene Symbol: STOML2
STOML2
0.040 Biomarker disease BEFREE Paratarg-7 (P-7) is a frequent paraprotein target in monoclonal gammopathy of undetermined significance (MGUS), multiple myeloma (MM), and Waldenström macroglobulinemia. 21586751 2011
Entrez Id: 30968
Gene Symbol: STOML2
STOML2
0.040 Biomarker disease BEFREE The dominant inheritance of pP-7 explains cases of familial IgM-MGUS/WM and enables the identification of family members at increased risk. 21220746 2011