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CCND1 and multiple myeloma are reported together in 1 article.
Gene
CCND1
- HGNC
- HGNC:1582
39articles
39mentions
2variants with confirmed gene link
Most co-reported phenotypes (articles)
colorectal cancer 9breast cancer 8leukemia 3prostate cancer 2Parkinson disease 1diabetes mellitus 1hepatitis B 1hepatocellular carcinoma 1
Reported variants (articles · ClinVar status)
Phenotype
Multiple myeloma
63articles
63mentions
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
1 records shown · first 60A diagnostic approach to detect cytogenetic heterogeneity and its prognostic significance in multiple myeloma.
PMID 37206191 | PMCID PMC10189271 | DOI 10.1016/j.jtumed.2023.03.009 · Journal of Taibah University Medical Sciences · 2023 · 4 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | CCND1 | “METHODS: Bone marrow aspirates were obtained from 72 patients with MM and evaluated by conventional cytogenetics (CCs) and interphase fluorescence in situ hybridization (iFISH) techniques for a panel of probes, including immunoglobulin heavy chain (IgH)/CCND1, IgH/fibroblast growth factor receptor 3 (FGFR3), IgH/MAFB, 13q deletion, and deletion 17p.” | 0.98 | hgnc_dict_v1 |
| phenotype | multiple myeloma | “A diagnostic approach to detect cytogenetic heterogeneity and its prognostic significance in multiple myeloma.” | 0.98 | phenotype_alias_lexicon_v2 |
| gene | FGFR3 | “METHODS: Bone marrow aspirates were obtained from 72 patients with MM and evaluated by conventional cytogenetics (CCs) and interphase fluorescence in situ hybridization (iFISH) techniques for a panel of probes, including immunoglobulin heavy chain (IgH)/CCND1, IgH/fibroblast growth factor receptor 3 (FGFR3), IgH/MAFB, 13q deletion, and deletion 17p.” | 0.98 | hgnc_dict_v1 |
| gene | MAFB | “METHODS: Bone marrow aspirates were obtained from 72 patients with MM and evaluated by conventional cytogenetics (CCs) and interphase fluorescence in situ hybridization (iFISH) techniques for a panel of probes, including immunoglobulin heavy chain (IgH)/CCND1, IgH/fibroblast growth factor receptor 3 (FGFR3), IgH/MAFB, 13q deletion, and deletion 17p.” | 0.98 | hgnc_dict_v1 |