PSMF1
HGNC:9571 · SaudiVarKB evidence summary derived from retained literature mentions.
3Gene mentions
3Publications
0Linked variants
2Associated phenotypes
Associated phenotypes
Co-mentioned in PSMF1 publications| Phenotype | Identifier | Articles | Mentions |
|---|---|---|---|
| Parkinson disease | — | 2 | 2 |
| breast cancer | — | 1 | 1 |
Linked variants
Variants normalized to PSMF1| Variant | HGVS / rsID | Articles | Mentions |
|---|
No normalized variants are linked to this gene.
Population context
Reported in the same publications| Country / region | Group | Cohort | Articles |
|---|---|---|---|
| Not specified | — | 24 | 1 |
| Not specified | — | 25 | 1 |
Supporting publications
3 records- 2026Variants in the proteasome regulator PSMF1 cause a phenotypic spectrum from parkinsonism to perinatal lethality.Nature communications1 mentions
- 2025Variants in the proteasome regulator PSMF1 cause a phenotypic spectrum from early-onset Parkinson's disease to perinatal lethality and disrupt mitochondrial function.medRxiv : the preprint server for health sciences1 mentions
- 2024Exploring a novel four-gene system as a diagnostic and prognostic biomarker for triple-negative breast cancer, using clinical variables.Computational biology and chemistry1 mentions