WIPF3
Description
The WIPF3 (WAS/WASL interacting protein family member 3) is a protein-coding gene located on chromosome 7.
WIPF3 may play a role in regulating the organization of the cytoskeleton within cells. It is also suspected to be involved in spermatogenesis, although this is based on similarity to other proteins.
WIPF3 is also known as CR16.
Associated Diseases
- male infertility with teratozoospermia due to single gene mutation
- partial chromosome Y deletion
- spermatogenic failure 20
- spermatogenic failure 72
- spermatogenic failure 27
- spermatogenic failure 18
- spermatogenic failure 46
- spermatogenic failure 42
- spermatogenic failure, X-linked, 3
- spermatogenic failure 65
- spermatogenic failure 43
- spermatogenic failure 49
- spermatogenic failure 19
- spermatogenic failure 45
- spermatogenic failure 40
- spermatogenic failure 5
