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GATA2 and intellectual disability are reported together in 1 article.
Gene
GATA2
- HGNC
- HGNC:4171
11articles
11mentions
0variants with confirmed gene link
Most co-reported phenotypes (articles)
Phenotype
Intellectual disability
- HPO
- HP:0001249
736articles
736mentions
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 60Identification of cell specific biomarkers for intellectual disability via single cell RNA sequencing and transcriptomic bioinformatics approaches.
PMID 40399537 | PMCID PMC12095737 | DOI 10.1038/s41598-025-85162-4 · Scientific reports · 2025 · 13 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | GATA2 | “Through the analysis of the regulatory network, we have identified several crucial transcriptional factors (TFs) including FOXC1, FOXL1, and GATA2; microRNAs such as mir-92a-3p, and mir-16-5p were investigated by procedural data analysis.” | 0.98 | hgnc_dict_v1 |
| phenotype | intellectual disability | “Identification of cell specific biomarkers for intellectual disability via single cell RNA sequencing and transcriptomic bioinformatics approaches.” | 0.98 | phenotype_alias_lexicon_v2 |
| gene | CD4 | “Specific genetic disorders that result in ID can also have immune system anomalies, such as changes in T (CD4+ and CD8+) cell activity.” | 0.98 | hgnc_dict_v1 |
| gene | RPS27A | “In this investigation, six ribosomal proteins (RPS27A, RPS21, RPS18, RPS7, RPS5, and RPL9) have been identified as the hub genes of ID from PPI.” | 0.98 | hgnc_dict_v1 |