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RAD51 and neurodevelopmental disorder are reported together in 1 article.
Gene
RAD51
- HGNC
- HGNC:9817
24articles
24mentions
3variants with confirmed gene link
Most co-reported phenotypes (articles)
breast cancer 11COVID-19 1SARS 1hepatocellular carcinoma 1inflammatory bowel disease 1lung cancer 1neurodevelopmental disorder 1ovarian cancer 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 60Defining the Genetic Landscape of Congenital Mirror Movements in 80 Affected Individuals.
PMID 38314870 | DOI 10.1002/mds.29669 · Movement disorders : official journal of the Movement Disorder Society · 2024 · 9 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | RAD51 | “To date, five genes have been associated with CMM, namely DCC, RAD51, NTN1, ARHGEF7, and DNAL4.” | 0.98 | hgnc_dict_v1 |
| phenotype | neurodevelopmental disorder | “BACKGROUND: Congenital mirror movements (CMM) is a rare neurodevelopmental disorder characterized by involuntary movements from one side of the body that mirror voluntary movements on the opposite side.” | 0.98 | phenotype_alias_lexicon_v2 |
| gene | DCC | “To date, five genes have been associated with CMM, namely DCC, RAD51, NTN1, ARHGEF7, and DNAL4.” | 0.98 | hgnc_dict_v1 |
| gene | NTN1 | “To date, five genes have been associated with CMM, namely DCC, RAD51, NTN1, ARHGEF7, and DNAL4.” | 0.98 | hgnc_dict_v1 |