ASXL1
HGNC:18318 · SaudiVarKB evidence summary derived from retained literature mentions.
8Gene mentions
8Publications
0Linked variants
3Associated phenotypes
Associated phenotypes
Co-mentioned in ASXL1 publications| Phenotype | Identifier | Articles | Mentions |
|---|---|---|---|
| leukemia | — | 3 | 3 |
| stroke | — | 1 | 1 |
| myocardial infarction | — | 1 | 1 |
Linked variants
Variants normalized to ASXL1| 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 | — | 60 | 1 |
| Not specified | — | 1,514 | 1 |
Supporting publications
8 records- 2026CHIP In cardiovascular and immune ageing.Ageing research reviews1 mentions
- 2025Unusual presentation and management of parathyroid carcinoma with pulmonary metastasis: a case report.AME case reports1 mentions
- 2025Impaired DNA damage responses and inflammatory signaling underpin hematopoietic stem cell defects in Gata2 haploinsufficiency.Stem cell reports1 mentions
- 2024Clinical Validation of the Somatic FANCD2 Mutation (c.2022-5C>T) as a Novel Molecular Biomarker for Early Disease Progression in Chronic Myeloid Leukemia: A Case-Control Study.Hematology reports1 mentions
- 2023Triple-Negative Primary Myelofibrosis: A Bone Marrow Pathology Group Study.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc1 mentions
- 2021Gene Expression Analysis of Pediatric Acute Myeloid Leukemia Identified a Hyperactive ASXL1/BAP1 Axis Linked with Poor Prognosis and over Expressed Epigenetic Modifiers.Pediatric hematology and oncology1 mentions
- 2020A Personalized Prediction Model for Outcomes after Allogeneic Hematopoietic Cell Transplant in Patients with Myelodysplastic Syndromes.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation1 mentions
- 2017A Children's Oncology Group and TARGET initiative exploring the genetic landscape of Wilms tumor.Nature genetics1 mentions