GCNT2
HGNC:4204 · SaudiVarKB evidence summary derived from retained literature mentions.
2Gene mentions
2Publications
0Linked variants
1Associated phenotypes
Associated phenotypes
Co-mentioned in GCNT2 publications| Phenotype | Identifier | Articles | Mentions |
|---|---|---|---|
| congenital cataract | — | 2 | 2 |
Linked variants
Variants normalized to GCNT2| 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 | — | — | 1 |
| Saudi Arabia | — | 26 | 1 |
Supporting publications
2 records- 2016Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts.PloS onePubMed ↗
- 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 ↗