PRR19
Description
The PRR19 (proline rich 19) is a protein-coding gene located on chromosome 19.
PRR19 promotes the formation of meiotic crossovers by interacting with CNTD1. It plays a role in the crossover differentiation step, which involves the conversion of crossover-specific recombination intermediates into mature crossovers.
PRR19 is also known as -.
Associated Diseases
- male infertility with teratozoospermia due to single gene mutation
- partial chromosome Y deletion
- spermatogenic failure 25
- congenital bilateral absence of vas deferens
- spermatogenic failure 65
- spermatogenic failure, X-linked, 3
- spermatogenic failures 50
- spermatogenic failure 39
- spermatogenic failure 40
- spermatogenic failure 72
- isochromosomy Yp
- spermatogenic failure 47
- spermatogenic failure 46
- spermatogenic failure 18
- spermatogenic failure 27
- spermatogenic failure 42
- spinocerebellar ataxia type 32
- spermatogenic failure 51
- spermatogenic failure 63
- spermatogenic failure 48
- spermatogenic failure 20
- spermatogenic failure 41
- spermatogenic failure 45
