Protein Information

Cytoscape View


UniProt AC / UniProt ID P31994 / FCG2B_HUMAN
Protein Name Low affinity immunoglobulin gamma Fc region receptor II-b precursor
Gene Name Name: FCGR2B
Synonyms:CD32,FCG2,IGFR2;
Organism Homo sapiens (Human)

PRO ID PR:P31994
DAG View
PRO Name low affinity immunoglobulin gamma Fc region receptor II-b (human)
Definition A low affinity immunoglobulin gamma Fc region receptor II-b that is encoded in the genome of human.
Short Label hFCGR2B
Category organism-gene

Interactive Sequence View

Select/align proteoforms across species


P31994 (FCGR2B) as Substrate



Site PTM Type PTM Enzyme Score Source PMID
N180 N-Glycosylation GlyGen 24190977
N187 N-Glycosylation GlyGen 24190977
N199 N-Glycosylation GlyGen 24190977
Y292 Phosphorylation IntAct   neXtProt   phospho.ELM   PhosphoSitePlus   RLIMS-P   UniProt 8756631, 33409482, 10382761, ...8577729, 9603468, 10704309, 9148918
Y292 Phosphorylation P06241 (FYN) PhosphoSitePlus 10704309
Y292 Phosphorylation P07948 (LYN) phospho.ELM   PhosphoSitePlus 8756631
Y292 Phosphorylation P51451 (BLK) neXtProt   phospho.ELM   PhosphoSitePlus 8756631
S293 Phosphorylation PhosphoSitePlus
Site PTM Type PTM Enzyme Score Source PMID
Y292 Phosphorylation HPRD 8756631
Y292 Phosphorylation P07948 (LYN) HPRD 8756631
Y292 Phosphorylation P51451 (BLK) HPRD 8756631
S293 Phosphorylation HPRD 20166139
Site PTM Type PTM Enzyme Score Source PMID
S253 Phosphorylation PhosphoSitePlus
Y273 Phosphorylation HPRD   PhosphoSitePlus 8756631
Y273 Phosphorylation P07948 (LYN) HPRD 8756631
Y273 Phosphorylation P51451 (BLK) HPRD 8756631
S274 Phosphorylation HPRD 20166139
Site PTM Type PTM Enzyme Score Source PMID
Y291 Phosphorylation HPRD 8756631
Y291 Phosphorylation P07948 (LYN) HPRD 8756631
Y291 Phosphorylation P51451 (BLK) HPRD 8756631
S292 Phosphorylation HPRD 20166139
Site PTM Type PTM Enzyme Score Source PMID
Y272 Phosphorylation HPRD 8756631
Y272 Phosphorylation P07948 (LYN) HPRD 8756631
Y272 Phosphorylation P51451 (BLK) HPRD 8756631
S273 Phosphorylation HPRD 20166139


PTM sites affected in variants

Site Variant Source PMID Disease [Sample source]
N187 S187 Biomuta DOID:10534 / stomach cancer [ icgc ]