PhenoPlasm: a database of disruption phenotypes for malaria parasite genes
Related Experiment Video
Updated: Feb 1, 2026

Author Spotlight: Identifying Compensatory Pathways in Malaria Parasites Containing Hypomorphic Allele of Essential Protein Kinases
Published on: November 22, 2024
Theo Sanderson1, Julian C Rayner1
1Malaria Programme, Wellcome Trust Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.
Abstract:
Two decades after the first Plasmodium transfection, attempts have been made to disrupt more than 3,151 genes in malaria parasites, across five Plasmodium species. While results from rodent malaria transfections have been curated and systematised, empowering large-scale analysis, phenotypic data from human malaria parasite transfections currently exists as individual reports scattered across a the literature. To facilitate systematic analysis of published experimental genetic data across Plasmodium species, we have built PhenoPlasm ( http://www.phenoplasm.org), a database of phenotypes generated by transfection experiments in all Plasmodium parasites. The site provides a simple interface linking citation-backed Plasmodium reverse-genetic phenotypes to gene IDs. The database has been populated with phenotypic data on 367 P. falciparum genes, curated from 176 individual publications, as well as existing data on rodent Plasmodium species from RMgmDB and PlasmoGEM. This is the first time that all available data on P. falciparum transfection experiments has been brought together in a single place. These data are presented using ortholog mapping to allow a researcher interested in a gene in one species to see results across other Plasmodium species. The collaborative nature of the database enables any researcher to add new phenotypes as they are discovered. As an example of database utility, we use the currently available datasets to identify RAP (RNA-binding domain abundant in Apicomplexa)-domain containing proteins as crucial to parasite survival.
Insights
PhenoPlasm is a new database that consolidates malaria parasite transfection data. It enables cross-species analysis of gene functions, identifying essential proteins like RAP-domain containing proteins for parasite survival.
Area of Science:
- Malaria research
- Parasitology
- Genetics
Background:
- Over 3,151 genes have been targeted in malaria parasites across five species.
- Rodent malaria transfection data is systematized, but human malaria parasite data is fragmented.
- A need exists for a centralized resource for analyzing Plasmodium transfection phenotypes.
Purpose of the Study:
- To build PhenoPlasm, a comprehensive database of Plasmodium transfection phenotypes.
- To facilitate systematic, cross-species analysis of experimental genetic data.
- To link gene IDs with citation-backed phenotypes for Plasmodium parasites.
Main Methods:
- Developed PhenoPlasm (http://www.phenoplasm.org) to curate and integrate transfection phenotype data.
- Populated the database with 367 P. falciparum genes from 176 publications.
- Incorporated existing rodent Plasmodium data from RMgmDB and PlasmoGEM.
- Implemented ortholog mapping for cross-species gene comparison.
Main Results:
- PhenoPlasm centralizes all available P. falciparum transfection data.
- The database includes data for P. falciparum and rodent Plasmodium species.
- Ortholog mapping allows researchers to explore gene function across different Plasmodium species.
- Database utility demonstrated by identifying RAP-domain proteins as crucial for parasite survival.
Conclusions:
- PhenoPlasm is the first comprehensive database for Plasmodium transfection phenotypes.
- The database enables systematic analysis and discovery across Plasmodium species.
- PhenoPlasm supports collaborative data sharing and expansion.
- Identified RNA-binding domain abundant in Apicomplexa (RAP)-domain proteins as vital for parasite survival.
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