Environment-dependent landscapes of coding variant impacts on coproporphyrinogen oxidase
Warren van LoggerenbergiD, Haotian ZhangiD, Vignesh Senguttuvan, Michael James ChambersiD, Mailoan Panchalingam, Alireza RasoulzadehiD, Anna AxakovaiD, Marinella GebbiaiD, Robert J. DesnickiD, Bruce WangiD, Caroline SchmittiD, Laurent GouyaiD, Jordi To‐FiguerasiD, Alexander Wahl, İvet BahariD, Pemra DorukeriD, Frederick P. RothiD
Abstract
Hereditary coproporphyria (HCP) -- caused by variants in coproporphyrinogen oxidase (CPOX) -- can be diagnosed via genome sequencing. However, 74% of clinically-reported CPOX missense variants are classified as variants of uncertain significance (VUS) due to lack of evidence. CPOX variant classification is further complicated by environment-dependence: For example, the CPOX variant p.Asn272His (c.814A>C) is classified as benign yet has been associated with HCP-like symptoms in the context of mercury exposure. Here we measured the functional impact of nearly all possible CPOX amino acid substitutions in both the presence and absence of mercury. The resulting CPOX variant effect maps reflect known protein structure and mutational tolerance patterns while also offering new sequence-structure-function insights. Scores from this atlas not only distinguish pathogenic from benign variants but also identify mercury-dependent variant impacts, thus informing our clinical, structural, and functional understanding of CPOX deficiency and illustrating the value of systematic context-dependent multiplexed assays of genetic variant effects.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 0
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Loss-of-function Variants in CPT1C: No Support for a Causal Role in Hereditary Spastic Paraplegia
Rui Zhu, Lang Liu, … Ziv Gan‐Or·Movement DisordersPeer-reviewed·Nov 28, 2025
- Expanding clinical and variant spectrum of CBX1-related syndrome: Report of three novel cases
Graciela Carrollo, Shuhei Fujino, … Kosuke Izumi·medRxiv·Sep 28, 2026
- Variability in Human Drug Metabolizing Cytochrome P450 CYP2C9, CYP2C19 and CYP3A5 Activities Caused by Genetic Variations in Cytochrome P450 Oxidoreductase
M. N. R. Velazques, S. Parween, … A. V. Pandey·bioRxiv·May 17, 2019
- Pathogenic variants of the mitochondrial copper chaperones SCO1 and SCO2 reshape their respective interactomes and disrupt cellular phospholipid metabolism
Sampurna Ghosh, Zakery N. Baker, … Scot C. Leary·bioRxiv·Sep 24, 2026
- Systematically testing human HMBS missense variants to reveal mechanism and pathogenic variation
Warren van Loggerenberg, Shahin Sowlati‐Hashjin, … Frederick P. Roth·The American Journal of Human GeneticsPeer-reviewed·Sep 19, 2023
- Characterization of mutations causing steroid 21-hydroxylase 1 deficiency in Brazilian and Portuguese populations.
M. J. Prado, S. Singh, … A. V. Pandey·bioRxiv·Dec 7, 2021