PLS3
HGNC:9091 · SaudiVarKB evidence summary derived from retained literature mentions.
2Gene mentions
2Publications
0Linked variants
2Associated phenotypes
Associated phenotypes
Co-mentioned in PLS3 publications| Phenotype | Identifier | Articles | Mentions |
|---|---|---|---|
| spinal muscular atrophy | — | 1 | 1 |
| osteogenesis imperfecta | — | 1 | 1 |
Linked variants
Variants normalized to PLS3| 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 | — | 87 | 1 |
| Not specified | — | 34 | 1 |
Supporting publications
2 records- 2021Diagnostic utility of next-generation sequence genetic panel testing in children presenting with a clinically significant fracture history.Archives of osteoporosis1 mentions
- 2019Evaluation of the role of an antioxidant gene in NSC-34 motor neuron-like cells as a model of a motor neuron disease.Folia morphologica1 mentions