Publication for MS4A1 and CR2
| Species | Symbol | Function* | Entrez Gene ID* | Other ID | Gene coexpression |
CoexViewer |
|---|---|---|---|---|---|---|
| hsa | MS4A1 | membrane spanning 4-domains A1 | 931 | [link] | ||
| hsa | CR2 | complement C3d receptor 2 | 1380 |
| Pubmed ID | Priority | Text |
|---|---|---|
| 18366248 | 0.96 | CD20 mAb binding on freshly isolated B cells using flow cytometry with anti-CD20 mAbs and a PE-conjugated anti-CD21 mAb. |
| 0.78 | CD20 mAb B1 resulted in a decreased CD20/CD21 MFI ratio for three out of five patients (unpublished data). | |
| 0.67 | CD20 mAb binding intensity (MFI) was correlated to CD21 mAb binding intensity by calculating the ratio of CD20/CD21 MFI. | |
| 0.60 | CD20/CD21 mAb staining was calculated and served as a relative measure for CD20 expression. | |
| 24187614 | 0.96 | CD20+CD5+CD10+/-CD21+/-CD23+/-IgM+IgD+/- and CD38+, but once they have evolved to type 2 (BT2), they become CD20+CD5+/-CD21++CD23+/-IgM++IgD++ and CD38+/-. |
| 30116248 | 0.95 | CD21, CD40, LYN, MS4A1, ORAI1, PLCG2, PTPRC, and STIM1 deficiency attractors. |
| 0.87 | CD21, CD40, LYN, MS4A1, and PTPRC (Figure 4). | |
| 0.82 | CD21, CD40, CD81, IKKB, KRAS, LYN, MALT1, MS4A1, NEMO, NFKB1, NFKBIA, ORAI1, PI3K, PLCG2, PTPRC, STIM1, and WIPF1 deficiencies. | |
| 0.79 | CD21, CD40, LYN, MS4A1, and PTPRC PID attractors. | |
| 0.69 | CD21, CD40, CD81, IKKB, LYN, MALT1, MS4A1, NEMO, NFKB1, NFKBIA, ORAI1, PI3K, PLCG2, STIM1, and WIPF1 and knockin perturbation of CARD11 gain-of-function, KRAS, NFKBIA, and PI3K) attractors. | |
| 21450903 | 0.95 | B1 cells (fractionated into CD21+ (B121+) and CD21- (B121-) subsets). |
| 0.54 | CD21 identified two clear splenic B1 subsets, and D6active MZ B cells amongst IgMhiCD23loCD5- cells (Figure 5C). | |
| 21304587 | 0.94 | CD20+ B cells were further analyzed based on their CD21 and CD27 surface molecule expression. |
| 0.91 | CD20+ B cells based on CD27 and CD21 surface expression and their functional characteristics (e.g. IgG production). | |
| 0.90 | CD21+CD27+CD20+ B cells are memory B cells that can be activated and induced to proliferate and differentiate into antibody secreting cells via polyclonal activation without T cell help. | |
| 0.81 | CD20 in all B cell subsets, and upregulation of CD138 expression in DP CD21+CD27+ B cells. | |
| 29717110 | 0.94 | MS4A1 (CD20), ITGAX (CD11c), TBX21 (T-bet), CR2 (CD21), FCER2 (CD23), FCGR2B (CD32B), CD24, CD27, CD38, CD40 and IL-21R (Fig. 5c, Supplementary Note 1). |
| 28133792 | 0.93 | CD20, as well as IgM and IgD. Bone marrow B-cell emigrants maintain expression of the pre-B cell surface marker CD10, while expressing low levels of the complement receptor CD21. |
| 28567040 | 0.93 | CD20+ B cells (Figure 3C) and large CD21+ FDC networks (Figure 3G), indicating that despite the suppressive environment, activated B cells were still able to induce the differentiation of tumor-associated stromal cells into FDC. |
| 27641977 | 0.92 | CD21 displayed the strongest activity in blocking HCV binding to B cells, followed by anti-CD20, anti-CD35, and anti-CD81. |
| 0.86 | CD20 is one of major B cell markers, CD21 is also known as complement receptor 2, CD32 is receptor for Fc fragment of immunoglobulin G, CD35 is complement receptor 1, and CD55 is membrane-bound decay-accelerating factor for convertases of complement system. | |
| 28667164 | 0.92 | CD20+/HLADR+ /CD21-/CD27+) and resting (CD3-/CD20+/HLADR+/CD21+ /CD27+) memory B cell numbers remained constant until day 70. |
| 28735813 | 0.92 | CD20+ CD21Lo CD27- CD11cHi. |
| 25517315 | 0.90 | CD20, CD21 and CD22 levels and modulates various surface antigens, it does not substantially influence other targets for mAbs-mediated therapy, such as CD38, CD52 and CD19 (Fig. S6). |
| 25088080 | 0.87 | B-1 cells express CD11b, higher levels of IgM (sIgM), and low levels of secreted IgD (sIgD), CD21, CD23, and CD45R (B220). |
| 23826242 | 0.86 | CD20 markers, so we do not know what fraction of the CD19+IgD-CD27-CD21- MBC observed in this study are the "exhausted" atypical MBC (CD19+CD10-CD27-CD21-) described in patients with high level HIV viremia and in malaria-exposed individuals from other populations. |
| 27844106 | 0.86 | CD20 and CD22, several other biomarkers have been investigated as targets for RIT in lymphoma, including the human leukocyte antigen DR (HLA-DR), CD21, and CD37. |
| 29530739 | 0.86 | CD20+), Follicular B cells(CD23+), Plasma cells (CD138), Follicular Dendritic Cells (CD21+) and macrophage/monocytes (CD68+). |
| 30723574 | 0.86 | CD21-) and activated (CD86+) B cells were evaluated in CD19+/CD20+/CD45+ B cells. |
| 28063478 | 0.85 | CD20, CD21, CD22, CD27, CD40, CD45RA, CD79A, CD79B, and RAG-2 in the fetal liver, bone marrow, and spleen was measured at 90-120DG. |
| 22477523 | 0.79 | CD20, CD21 and CD81), each of which forms complexes with the B cell antigen receptor, appear to lower the threshold for B cell activation (Fig. 1). |
| 0.79 | CD20 and CD81, CD21, also known as CR2 due to its role as a complement receptor, focuses antigen activation on the BCR. | |
| 23455507 | 0.63 | B-1 cells, primate CD11b+ B cells expressed higher FSC, IgM, and CD19, and lower levels of CD21 relative to CD11b- B cells (Fig. 1C). |
| 23565504 | 0.60 | CD20, CD21, CD22, and CD30 (see Table 1 for an overview). |
| 31877281 | 0.56 | CD20+ cells and CD3+ cells segregated into anatomically distinct but adjacent zones, with a CD21+ follicular dendritic cell (FDC) network, CD23+ cells and BCL6 staining in the B cell zone (Figs. 1 and 2). |
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