| Species | Disruptability | Reference | Submitter | |
|---|---|---|---|---|
| P. falciparum 3D7 | 
											 Refractory  | 
                                            20466936 (Conditional) | Theo Sanderson, Wellcome Trust Sanger Institute | |
| P. falciparum 3D7 | 
											 Refractory  | 
                                            USF piggyBac screen (Insert. mut.) | USF PiggyBac Screen | |
| P. berghei ANKA | 
											 Refractory  | 
                                            RMgm-536 | Imported from RMgmDB | |
| P. berghei ANKA | 
											 Refractory  | 
                                            PlasmoGEM (Barseq) | PlasmoGEM | |
| Species | Stage | Phenotype | Reference | Submitter | 
|---|---|---|---|---|
| P. falciparum 3D7 | Asexual | 
											 Egress defect  | 
                                              29487234 (Knock down)
									 Micronemes fail to discharge  | 
                                            Theo Sanderson, Wellcome Trust Sanger Institute | 
| P. falciparum 3D7 | Asexual | 
											 Cell cycle arrest  | 
                                              28288121 (Conditional)
									 Knock sideways to the nucleus caused accumulation of segmented schizonts  | 
                                            Theo Sanderson, Wellcome Trust Sanger Institute | 
| P. falciparum 3D7 | Asexual | 
											 Egress defect  | 
                                            20466936 (Knock down) | Theo Sanderson, Francis Crick Institute | 
| P. falciparum 3D7 | Asexual | 
											 Difference from wild-type  | 
                                              31915223 (Knock down)
									 '58 phosphorylation sites on 50 proteins with significant reduction in levels of PfCDPK5-deficient parasites. Furthermore, gene ontology analysis of the identified proteins reveals enrichment in transmembrane- and membrane-associated proteins and in proteins associated with transport activity. Among the identified proteins is PfNPT1, a member of the apicomplexan-specific novel putative transporter (NPT) family of proteins.'  | 
                                            Theo Sanderson, Francis Crick Institute | 
 
							Localization and KS with protein targets. (a,b) Knockin cell lines of CDPK5-2×FKBP-GFP with an mCherry-tagged nuclear mislocalizer (MislocalizerN) (a) and HP1-2×FKBP-GFP with a plasma-membrane mislocalizer (MislocalizerP). In synchronized parasites, KS of CDPK5 caused an accumulation of segmented schizonts. (b). Representative fluorescence microscopy images of rapalog-treated and control cells (after 16 h). Mislocalization of HP1 caused an accumulation of gametocytes.Birnbaum J, Flemming S, Reichard N, Soares AB, Mesén-Ramírez P, Jonscher E, Bergmann B, Spielmann T. A genetic system to study Plasmodium falciparum protein function. Nat Methods. 2017 Mar 13.
See original on MMP| PlasmoDB | PF3D7_1337800 | 
| GeneDB | PF3D7_1337800 | 
| Malaria Metabolic Pathways | Localisation images Pathways mapped to  | 
                                            
                                        
| Previous ID(s) | PF13_0211 | 
| Orthologs | PBANKA_1351500 , PCHAS_1356100 , PKNH_1263500 , PVP01_1216900 , PVX_082820 , PY17X_1356700 | 
| Google Scholar | Search for all mentions of this gene |