# hereditary spastic paraplegia 57

> gene (3q12.2) encoding protein TFG, which is thought to play a role in ER microtubular architecture and function.

**Wikidata**: [Q32143215](https://www.wikidata.org/wiki/Q32143215)  
**Source**: https://4ort.xyz/entity/hereditary-spastic-paraplegia-57


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Inhibition of TFG function causes hereditary axon degeneration by impairing endoplasmic reticulum structure
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)