Igm Monoclonal Gammopathy Of Uncertain Significance

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Results for "Igm Monoclonal Gammopathy Of Uncertain Significance": 11 genes

Name
JCHAIN Gene joining chain of multimeric IgA and IgM Enables IgA binding activity and protein homodimerization activity. Contributes to several functions, including immunoglobulin receptor binding activity; peptidoglycan binding activity; and phosphatidylcholine binding activity. Involved in several processes, including glomerular filtration; innate immune response; and positive regulation of respiratory burst. Located in extracellular space. Part of monomeric IgA immunoglobulin complex; pentameric IgM immunoglobulin complex; and secretory dimeric IgA immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025]
FCAMR Gene Fc receptor, IgA, IgM, high affinity Predicted to enable IgA binding activity; IgM binding activity; and transmembrane signaling receptor activity. Predicted to be involved in signal transduction. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025]
FCMR Gene Fc fragment of IgM receptor Fc receptors specifically bind to the Fc region of immunoglobulins (Igs) to mediate the unique functions of each Ig class. FAIM3 encodes an Fc receptor for IgM (see MIM 147020) (Kubagawa et al., 2009 [PubMed 19858324]; Shima et al., 2010 [PubMed 20042454]).[supplied by OMIM, Jul 2010]
MSK32 Gene antigen identified by monoclonal* antibody K66*
MSK38 Gene antigen identified by monoclonal* antibody O5*
MIC12 Gene antigen identified by monoclonal* antibody 30.2A8*
MIC7 Gene antigen identified by monoclonal* antibody 28.3.7*
MER5 Gene antigen identified by monoclonal* antibody 2D8*
MSK9 Gene antigen identified by monoclonal* antibody K15*
MSK10 Gene antigen identified by monoclonal* antibody AJ425*
MFI2 Gene antigen p97 (melanoma associated) identified by monoclonal* antibodies 133.2 and 96.5* The protein encoded by this gene is a cell-surface glycoprotein found on melanoma cells. The protein shares sequence similarity and iron-binding properties with members of the transferrin superfamily. The importance of the iron binding function has not yet been identified. This gene resides in the same region of chromosome 3 as members of the transferrin superfamily. Alternative splicing results in two transcript variants. [provided by RefSeq, Jul 2008]