FOXL1
HGNC:3817 · SaudiVarKB evidence summary derived from retained literature mentions.
3Gene mentions
3Publications
0Linked variants
4Associated phenotypes
Associated phenotypes
Co-mentioned in FOXL1 publications| Phenotype | Identifier | Articles | Mentions |
|---|---|---|---|
| intellectual disability | HP:0001249 | 1 | 1 |
| diabetes mellitus | — | 1 | 1 |
| neurodevelopmental disorder | HP:0012759 | 1 | 1 |
| colorectal cancer | — | 1 | 1 |
Linked variants
Variants normalized to FOXL1| 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 | — | 577 | 1 |
Supporting publications
3 records- 2025Identification of cell specific biomarkers for intellectual disability via single cell RNA sequencing and transcriptomic bioinformatics approaches.Scientific reportsPubMed ↗
- 2023Identification of genetic biomarkers, drug targets and agents for respiratory diseases utilising integrated bioinformatics approaches.Scientific reportsPubMed ↗
- 2015A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer.Scientific reportsPubMed ↗