Details
| Type | Processed Transcript |
| Official Symbol | HERC2 |
| Official Name | HECT and RLD domain containing E3 ubiquitin protein ligase 2 [Source:HGNC Symbol;Acc:HGNC:4868] |
| Ensembl ID | ENSG00000277278 |
| Bio databases IDs | |
| Aliases | HECT and RLD domain containing E3 ubiquitin protein ligase 2 |
| Species | Human, Homo sapiens |
Pathways
Biological processes and signaling networks where the HERC2 gene in human plays a role, providing insight into its function and relevance in health or disease.
Top Findings
The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
phenotypes
- Mental retardation autosomal recessive 38
- PRADER-WILLI SYNDROME
- SKIN/HAIR/EYE PIGMENTATION VARIATION IN 1