Details
| Type | Protein Coding |
| Official Symbol | TWIST2 |
| Official Name | twist family bHLH transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:20670] |
| Ensembl ID | ENSG00000288335 |
| Bio databases IDs | |
| Aliases | twist family bHLH transcription factor 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
- Ablepharon-Macrostomia syndrome
- Barber-Say syndrome
- FOCAL FACIAL DERMAL DYSPLASIA 3 SETLEIS TYPE
- Ablepharon macrostomia syndrome
- SETLEIS SYNDROME