RHOXF1
Description
The RHOXF1 (Rhox homeobox family member 1) is a protein-coding gene located on chromosome X.
Rhox homeobox family member 1 is a protein encoded by the RHOXF1 gene in humans.
This transcription factor may play a role in reproductive processes, specifically by influencing the expression of genes involved in spermatogenesis.
RHOXF1 is also known as OTEX, PEPP1.
Associated Diseases
- male infertility with teratozoospermia due to single gene mutation
- partial chromosome Y deletion
- spermatogenic failure 8
- spermatogenic failure 1
- spermatogenic failure 25
- spermatogenic failure 48
- spermatogenic failure 51
- spermatogenic failure, X-linked, 3
- spermatogenic failure 40
- spermatogenic failure 63
- spermatogenic failure 47
- spermatogenic failure 22
- spermatogenic failure 39
- spermatogenic failure 65
- spermatogenic failure 70
- spermatogenic failure 41
- spermatogenic failure 10
- spermatogenic failure 11
- spermatogenic failures 50
- congenital bilateral absence of vas deferens
- spermatogenic failure 7
- spermatogenic failure 61
- spermatogenic failure 73
