SUCO
HGNC:1240 · SaudiVarKB evidence summary derived from retained literature mentions.
2Gene mentions
2Publications
0Linked variants
2Associated phenotypes
Associated phenotypes
Co-mentioned in SUCO publications| Phenotype | Identifier | Articles | Mentions |
|---|---|---|---|
| neurodevelopmental disorder | HP:0012759 | 1 | 1 |
| skeletal dysplasia | — | 1 | 1 |
Linked variants
Variants normalized to SUCO| 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 | — | 188 | 1 |
| Not specified | — | 411 | 1 |
Supporting publications
2 records- 2025Recessive genomic and phenotypic variation in consanguineous families with cerebral palsy.medRxiv : the preprint server for health sciencesPubMed ↗
- 2018Expanding the phenome and variome of skeletal dysplasia.Genetics in medicine : official journal of the American College of Medical GeneticsPubMed ↗