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Gene profile

FGFR1

HGNC:3688 · SaudiVarKB evidence summary derived from retained literature mentions.

14Gene mentions
14Publications
3Linked variants
5Associated phenotypes

Associated phenotypes

Co-mentioned in FGFR1 publications
PhenotypeIdentifierArticlesMentions
breast cancer33
lymphoma11
colorectal cancer11
prostate cancer11
lung cancer11

Linked variants

Variants normalized to FGFR1
VariantHGVS / rsIDArticlesMentions
rs881300rs88130011
rs881299rs88129911
rs7829058rs782905811

Population context

Reported in the same publications
Country / regionGroupCohortArticles
Not specified01
Not specified61
Not specified1151
Not specified601
Not specified7671
Not specified4,4021

Supporting publications

14 records
  1. 2026Unusual morphologic features in molecularly defined high-grade sarcomas of the uterus.Annals of diagnostic pathologyPubMed ↗
  2. 2025Genomic Landscape of Advanced Solid Tumors in Middle East and North Africa Using Circulating Tumor DNA in Routine Clinical Practice.OncologyPubMed ↗
  3. 2025Analysing DNA methylation and transcriptomic signatures to predict prostate cancer recurrence risk.Discover oncologyPubMed ↗
  4. 2025Polymorphisms in SOX2/FGFR1 are associated with skeletal class III maxillary and mandibular dimensions: A preliminary study.Journal of Taibah University Medical SciencesPubMed ↗
  5. 2025Breast Cancer: Molecular Pathogenesis and Targeted Therapy.MedCommPubMed ↗
  6. 2024A comprehensive overview of selective and novel fibroblast growth factor receptor inhibitors as a potential anticancer modality.Acta pharmaceutica (Zagreb, Croatia)PubMed ↗
  7. 2023Mutations in FGFR1 were associated with growth traits in sheep (Ovis aries).Animal biotechnologyPubMed ↗
  8. 2023Genetic Influence of Fracture Nonunion (FNU): A Systematic Review.Pharmacogenomics and personalized medicinePubMed ↗
  9. 2023Myeloid and lymphoid neoplasm with novel complex translocation: unusual case report with T-lymphoblastic lymphoma, myeloid hyperplasia, eosinophilia, basophilia, and t(1;8;10)( (p31;q24;q11.2).Journal of hematopathologyPubMed ↗
  10. 2022Therapeutic Targeting of FGFR Signaling in Head and Neck Cancer.Cancer journal (Sudbury, Mass.)PubMed ↗
  11. 2022De Novo Heterozygous Mutation in FGFR2 Causing Type II Pfeiffer Syndrome.Case reports in geneticsPubMed ↗
  12. 2021Elevated NSD3 histone methylation activity drives squamous cell lung cancer.NaturePubMed ↗
  13. 2016UGT2B4 previously implicated in the risk of breast cancer is associated with menarche timing in Ukrainian females.GenePubMed ↗
  14. 2014Epigenome-wide DNA methylation in hearing ability: new mechanisms for an old problem.PloS onePubMed ↗