CCNO
HGNC:18576 · SaudiVarKB evidence summary derived from retained literature mentions.
3Gene mentions
3Publications
0Linked variants
3Associated phenotypes
Associated phenotypes
Co-mentioned in CCNO publications| Phenotype | Identifier | Articles | Mentions |
|---|---|---|---|
| primary ciliary dyskinesia | — | 2 | 2 |
| infertility | — | 1 | 1 |
| recurrent pregnancy loss | — | 1 | 1 |
Linked variants
Variants normalized to CCNO| 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 | — | 16 | 1 |
Supporting publications
3 records- 2024Novel CYCLIN-O pathogenic variants in a patient presenting with bronchiectasis secondary to reduced generation of multiple motile cilia.Respirology case reportsPubMed ↗
- 2020A genomics approach to females with infertility and recurrent pregnancy loss.Human geneticsPubMed ↗
- 2014Mutations in CCNO result in congenital mucociliary clearance disorder with reduced generation of multiple motile cilia.Nature geneticsPubMed ↗