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 |
Pathways
Biological processes and signaling networks where the TWIST2 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
- Ablepharon-Macrostomia syndrome
- Barber-Say syndrome
- FOCAL FACIAL DERMAL DYSPLASIA 3 SETLEIS TYPE
- Ablepharon macrostomia syndrome
- SETLEIS SYNDROME