NEIL1
HGNC:18448 · SaudiVarKB evidence summary derived from retained literature mentions.
3Gene mentions
3Publications
0Linked variants
5Associated phenotypes
Associated phenotypes
Co-mentioned in NEIL1 publications| Phenotype | Identifier | Articles | Mentions |
|---|---|---|---|
| intellectual disability | HP:0001249 | 1 | 1 |
| ovarian cancer | — | 1 | 1 |
| nephrotic syndrome | — | 1 | 1 |
| dyslipidemia | — | 1 | 1 |
| breast cancer | — | 1 | 1 |
Linked variants
Variants normalized to NEIL1| Variant | HGVS / rsID | Articles | Mentions |
|---|
No normalized variants are linked to this gene.
Population context
Reported in the same publications| Country / region | Group | Cohort | Articles |
|---|---|---|---|
| Not specified | — | 15 | 1 |
| Not specified | — | 139 | 1 |
| Saudi Arabia | — | 62 | 1 |
Supporting publications
3 records- 2025Familial vs sporadic normal pressure hydrocephalus: a comparative study.Journal of neurologyPubMed ↗
- 2023Genetic analyses of DNA repair pathway associated genes implicate new candidate cancer predisposing genes in ancestrally defined ovarian cancer cases.Frontiers in oncologyPubMed ↗
- 2013A molecular genetic analysis of childhood nephrotic syndrome in a cohort of Saudi Arabian families.Journal of human geneticsPubMed ↗