YIPF5
Description
YIPF5, also known as ‘Yipf5 interacting protein with ankyrin repeats‘, is a gene located on chromosome 17 in humans. It encodes a protein involved in various cellular processes, primarily focusing on regulating protein turnover and maintaining cellular homeostasis. The protein interacts with other proteins like Yipf5 and ankyrin repeat-containing proteins, contributing to complex signaling pathways. Its importance in maintaining cellular health is highlighted by its involvement in several diseases, and recent research is uncovering its role in specific disease pathways.
Associated Diseases
- Neurodevelopmental Disorders: YIPF5 mutations have been associated with intellectual disability and autism spectrum disorder.
- Cancer: Emerging evidence suggests a link between YIPF5 alterations and certain cancers, such as leukemia and lymphoma.
Did you know?
The YIPF5 gene is highly conserved across various species, indicating its importance in fundamental cellular functions.
