Details
| Type | Protein Coding |
| Official Symbol | PCGF2 |
| Official Name | polycomb group ring finger 2 [Source:HGNC Symbol;Acc:HGNC:12929] |
| Ensembl ID | ENSG00000278644 |
| Bio databases IDs | |
| Aliases | polycomb group ring finger 2 |
| Species | Human, Homo sapiens |
Top Findings
The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
phenotypes
- TURNPENNY-FRY SYNDROME
- Craniofacial Neurological Cardiovascular and Skeletal Features
- Intellectual disability