| Primary Identifier | IPR040111 | Type | Family |
| Short Name | ODAD4 |
| description | ODAD4 (also known as TTC25) is a subunit of the outer dynein arm (ODA) docking complex (DC). Mutations of the TTC25 gene cause an ODA-DC defect involving severely reduced ciliary motility and classical symptoms of PCD (primary ciliary dyskinesia), as well as randomization of left-right body asymmetry in humans and mice []. |
