Details
| Type | Protein Coding |
| Official Symbol | Wdr62 |
| Official Name | WD repeat domain 62 [Source:RGD Symbol;Acc:1306714] |
| Ensembl ID | ENSRNOG00000049708 |
| Bio databases IDs | |
| Aliases | WD repeat domain 62 |
| Species | Rat, Rattus norvegicus |
Top Findings
The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
phenotypes
- Dwarfism
- Polymicrogyria
- Intellectual Disability
- microcephaly
- primary autosomal recessive microcephaly