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Gene profile

NPM1

HGNC:7910 · SaudiVarKB evidence summary derived from retained literature mentions.

15Gene mentions
15Publications
1Linked variants
3Associated phenotypes

Associated phenotypes

Co-mentioned in NPM1 publications
PhenotypeIdentifierArticlesMentions
leukemia1313
lymphoma11
Noonan syndrome11

Linked variants

Variants normalized to NPM1
VariantHGVS / rsIDArticlesMentions
S34F11

Population context

Reported in the same publications
Country / regionGroupCohortArticles
Saudi Arabia · Jeddah871
Not specified301
Not specified151
Not specified351
Not specified1311
Not specified781
Not specified1,8881
Not specified6001

Supporting publications

15 records
  1. 2026The impact of DNMT3A mutation on survival of AML patients receiving allotransplant in first remission depends on the karyotype and co-occurring mutations.Bone marrow transplantation1 mentions
  2. 2026Targeting the Menin-KMT2A Interface: Medicinal Chemistry Rules Governing Reversible, Covalent, and Degrader Inhibitors.Chemical biology & drug design1 mentions
  3. 2026Epigenetics and In Silico Transcriptome Analysis of Pediatric Acute Myeloid Leukemia.European journal of haematology1 mentions
  4. 2025Molecular Analysis of Genes CEBPA, NPM1, IDH1, and RUNX1 Polymorphisms as Biomarker Potential in Leukemia Patients.Molecular carcinogenesis1 mentions
  5. 2025HOX-PBX Up-regulation Predicts Favorable Prognosis in NPM1-mutated Normal Cytogenetic AML via WNT Signaling.Anticancer research1 mentions
  6. 2024Application of Newly Customized Myeloid NGS Panel in the Diagnosis of Myeloid Malignancies.International journal of general medicine1 mentions
  7. 2024An Ultra-Fast Validated Green UPLC-MS/MS Approach for Assessing Revumenib in Human Liver Microsomes: In Vitro Absorption, Distribution, Metabolism, and Excretion and Metabolic Stability Evaluation.Medicina (Kaunas, Lithuania)1 mentions
  8. 2022Decreased CD177pos neutrophils in myeloid neoplasms is associated with NPM1, RUNX1, TET2, and U2AF1 S34F mutations.Leukemia research1 mentions
  9. 2021Prognostic relevance of combined IDH1 and NPM1 mutations in the intermediate cytogenetic de novo acute myeloid leukemia.Cellular and molecular biology (Noisy-le-Grand, France)1 mentions
  10. 2020Comprehensive Genomic Analysis of Noonan Syndrome and Acute Myeloid Leukemia in Adults: A Review and Future Directions.Acta haematologica1 mentions
  11. 2019Overall survival of adult acute myeloid leukemia based on cytogenetic and molecular abnormalities during 5 years in a single center study.Saudi medical journal1 mentions
  12. 2013A surrogate marker to detect nucleophosnim (NPM1) gene mutations in the cytoplasm of acute myeloid leukemia (AML) blast cells in 30 adult Iraqi patients.Annals of Saudi medicine1 mentions
  13. 2013Novel t(7;10)(p22;p24) along with NPM1 mutation in patient with relapsed acute myeloid leukemia.Annals of Saudi medicine1 mentions
  14. 2011Detection of nucleophosmin and FMS-like tyrosine kinase-3 gene mutations in acute myeloid leukemia.Annals of Saudi medicine1 mentions
  15. 2008The challenge of risk stratification in acute myeloid leukemia with normal karyotype.Hematology/oncology and stem cell therapy1 mentions