TTC17
Description
The TTC17 (tetratricopeptide repeat domain 17) is a protein-coding gene located on chromosome 11.
TTC17 plays a role in primary ciliogenesis by regulating the assembly of actin filaments.
TTC17 is also known as -.
Associated Diseases
- migraine disorder
- refractive error
- breast cancer
- X-linked retinal dysplasia
- severe early-childhood-onset retinal dystrophy
- hypertriglyceridemia 2
- age related macular degeneration 11
- age related macular degeneration 4
- age related macular degeneration 7
- cholesterol-ester transfer protein deficiency