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CSF3R and leukemia are reported together in 2 articles.
Gene
CSF3R
- HGNC
- HGNC:2439
4articles
4mentions
0variants with confirmed gene link
Most co-reported phenotypes (articles)
Phenotype
Leukemia
652articles
652mentions
12co-reported genes shown
Most co-reported genes (articles)
Counts are literature co-mentions in SaudiVarKB, not clinical or causal assertions. Gene details: HGNC; variant status: ClinVar via dbSNP.
Publications
2 records shown · first 60Chronic Neutrophilic Leukemia with Monocytosis.
PMID 34123950 | PMCID PMC8191347 | DOI 10.12890/2021_002595 · European journal of case reports in internal medicine · 2021 · 5 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | CSF3R | “The revised WHO criteria 2016 included CSF3R gene mutations as a diagnostic finding.” | 0.98 | hgnc_dict_v1 |
| phenotype | leukemia | “Chronic Neutrophilic Leukemia with Monocytosis.” | 0.98 | phenotype_alias_lexicon_v2 |
| phenotype | coronary artery disease | “The patient's medical history was significant for coronary artery disease, hypertension, chronic obstructive pulmonary disease, bilateral cystic bronchiectasis, moderate pulmonary hypertension, tuberculosis treated 27 years previously, hypothyroidism, and a thyroid nodule.” | 0.98 | phenotype_alias_lexicon_v2 |
| phenotype | hypertension | “The patient's medical history was significant for coronary artery disease, hypertension, chronic obstructive pulmonary disease, bilateral cystic bronchiectasis, moderate pulmonary hypertension, tuberculosis treated 27 years previously, hypothyroidism, and a thyroid nodule.” | 0.98 | phenotype_alias_lexicon_v2 |
Identification of CSF3R Mutations in B-Lineage Acute Lymphoblastic Leukemia Using Comprehensive Cancer Panel and Next-Generation Sequencing.
PMID 34573308 | PMCID PMC8470887 | DOI 10.3390/genes12091326 · Genes · 2021 · 5 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | CSF3R | “Identification of CSF3R Mutations in B-Lineage Acute Lymphoblastic Leukemia Using Comprehensive Cancer Panel and Next-Generation Sequencing.” | 0.98 | hgnc_dict_v1 |
| phenotype | leukemia | “Identification of CSF3R Mutations in B-Lineage Acute Lymphoblastic Leukemia Using Comprehensive Cancer Panel and Next-Generation Sequencing.” | 0.98 | phenotype_alias_lexicon_v2 |
| variant | S661N | “Our results describe new mutations in CSF3R gene including S661N, S557G, and Q170X which might be associated with disease progression.” | 0.82 | literature_variant_regex_v2 |
| variant | S557G | “Our results describe new mutations in CSF3R gene including S661N, S557G, and Q170X which might be associated with disease progression.” | 0.82 | literature_variant_regex_v2 |