FN1
HGNC:3778 · SaudiVarKB evidence summary derived from retained literature mentions.
10Gene mentions
10Publications
0Linked variants
8Associated phenotypes
Associated phenotypes
Co-mentioned in FN1 publications| Phenotype | Identifier | Articles | Mentions |
|---|---|---|---|
| obesity | HP:0001513 | 1 | 1 |
| epilepsy | HP:0001250 | 1 | 1 |
| diabetes mellitus | — | 1 | 1 |
| coronary artery disease | — | 1 | 1 |
| dyslipidemia | — | 1 | 1 |
| inflammatory bowel disease | — | 1 | 1 |
| systemic lupus erythematosus | — | 1 | 1 |
| breast cancer | — | 1 | 1 |
Linked variants
Variants normalized to FN1| 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 | — | 34 | 1 |
| Saudi Arabia | — | 100 | 1 |
| Not specified | — | 265 | 1 |
Supporting publications
10 records- 2026Inflammatory Myofibroblastic Tumor of Adults ≥40 Years: A Clinicopathologic Study of 34 Cases.The American journal of surgical pathologyPubMed ↗
- 2025Identification of adipose-proximal biomarkers in breast cancer using weighted gene co-expression network analysis.ProtoplasmaPubMed ↗
- 2023Utilizing Andrographis paniculata leaves and roots by effective usage of the bioactive andrographolide and its nanodelivery: investigation of antikindling and antioxidant activities through in silico and in vivo studies.Frontiers in nutritionPubMed ↗
- 2023Elucidation of genetic determinants of dyslipidaemia using a global screening array for the early detection of coronary artery disease.Mammalian genome : official journal of the International Mammalian Genome SocietyPubMed ↗
- 2023Using CADD tools to inhibit the overexpressed genes FAP, FN1, and MMP1 by repurposing ginsenoside C and Rg1 as a treatment for oral cancer.Frontiers in molecular biosciencesPubMed ↗
- 2022Integrative system biology and mathematical modeling of genetic networks identifies shared biomarkers for obesity and diabetes.Mathematical biosciences and engineering : MBEPubMed ↗
- 2022Exome Sequencing Identifies the Extremely Rare ITGAV and FN1 Variants in Early Onset Inflammatory Bowel Disease Patients.Frontiers in pediatricsPubMed ↗
- 2021Construction of miRNA-mRNA network for the identification of key biological markers and their associated pathways in IgA nephropathy by employing the integrated bioinformatics analysis.Saudi journal of biological sciencesPubMed ↗
- 2019Identification of important invasion and proliferation related genes in adrenocortical carcinoma.Medical oncology (Northwood, London, England)PubMed ↗
- 2017Fibronectin glomerulopathy - A sporadic case with unusual clinical manifestation.Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi ArabiaPubMed ↗