WDR87
HGNC:29934 · SaudiVarKB evidence summary derived from retained literature mentions.
2Gene mentions
2Publications
0Linked variants
3Associated phenotypes
Associated phenotypes
Co-mentioned in WDR87 publications| Phenotype | Identifier | Articles | Mentions |
|---|---|---|---|
| congenital cataract | — | 2 | 2 |
| developmental delay | HP:0001263 | 1 | 1 |
| cleft lip and palate | — | 1 | 1 |
Linked variants
Variants normalized to WDR87| 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 |
|---|---|---|---|
| Saudi Arabia | — | 26 | 1 |
| Not specified | — | 166 | 1 |
Supporting publications
2 records- 2017Novel phenotypes and loci identified through clinical genomics approaches to pediatric cataract.Human geneticsPubMed ↗
- 2015Phenotypes of Recessive Pediatric Cataract in a Cohort of Children with Identified Homozygous Gene Mutations (An American Ophthalmological Society Thesis).Transactions of the American Ophthalmological SocietyPubMed ↗