EXOC3L2
HGNC:30162 · SaudiVarKB evidence summary derived from retained literature mentions.
2Gene mentions
2Publications
0Linked variants
1Associated phenotypes
Associated phenotypes
Co-mentioned in EXOC3L2 publications| Phenotype | Identifier | Articles | Mentions |
|---|---|---|---|
| Bardet-Biedl syndrome | — | 1 | 1 |
Linked variants
Variants normalized to EXOC3L2| 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 | — | 44 | 1 |
| Not specified | — | 371 | 1 |
Supporting publications
2 records- 2018Molecular autopsy in maternal-fetal medicine.Genetics in medicine : official journal of the American College of Medical GeneticsPubMed ↗
- 2016Characterizing the morbid genome of ciliopathies.Genome biologyPubMed ↗