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DRD2 and neurodevelopmental disorder are reported together in 1 article.
Gene
DRD2
- HGNC
- HGNC:3023
12articles
12mentions
5variants with confirmed gene link
Most co-reported phenotypes (articles)
Alzheimer disease 2Parkinson disease 2autism spectrum disorder 2breast cancer 1intellectual disability 1neurodevelopmental disorder 1obesity 1
Reported variants (articles · ClinVar status)
Phenotype
Neurodevelopmental disorder
- HPO
- HP:0012759
450articles
450mentions
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 60Gene-gene and gene-environmental interaction of dopaminergic system genes in Pakistani children with attention deficit hyperactivity disorder.
PMID 39050560 | PMCID PMC11268355 | DOI 10.1016/j.sjbs.2024.104045 · Saudi journal of biological sciences · 2024 · 8 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | DRD2 | “This study examined the specific gene variants, dopamine transporter 1 (DAT1) rs6350, dopamine receptor D3 (DRD3) rs6280, dopamine receptor D2 (DRD2) rs6277, and catechol-O-methyltransferase (COMT) rs4633, in relation to ADHD among Pakistani children by exploring the potential gene-gene and gene-environment interactions.” | 0.98 | hgnc_dict_v1 |
| phenotype | neurodevelopmental disorder | “BACKGROUND: Attention deficit hyperactivity disorder (ADHD) is a neurodevelopmental disorder influenced by genetic and environmental factors.” | 0.98 | phenotype_alias_lexicon_v2 |
| gene | DRD3 | “This study examined the specific gene variants, dopamine transporter 1 (DAT1) rs6350, dopamine receptor D3 (DRD3) rs6280, dopamine receptor D2 (DRD2) rs6277, and catechol-O-methyltransferase (COMT) rs4633, in relation to ADHD among Pakistani children by exploring the potential gene-gene and gene-environment interactions.” | 0.98 | hgnc_dict_v1 |
| gene | COMT | “This study examined the specific gene variants, dopamine transporter 1 (DAT1) rs6350, dopamine receptor D3 (DRD3) rs6280, dopamine receptor D2 (DRD2) rs6277, and catechol-O-methyltransferase (COMT) rs4633, in relation to ADHD among Pakistani children by exploring the potential gene-gene and gene-environment interactions.” | 0.98 | hgnc_dict_v1 |