SWSAP1
Description
The SWSAP1 (SWIM-type zinc finger 7 associated protein 1) is a protein-coding gene located on chromosome 19.
SWSAP1 is also known as C19orf39, SWS1AP1, ZSWIM7AP1.
Associated Diseases
- partial chromosome Y deletion
- male infertility with teratozoospermia due to single gene mutation
- isolated congenital hypogonadotropic hypogonadism
- spermatogenic failure, X-linked, 2
- 46,XX testicular disorder of sex development
- 46,XY complete gonadal dysgenesis
- spinocerebellar ataxia type 32
- congenital bilateral absence of vas deferens
- spermatogenic failure 25
- spermatogenic failures 50
- isochromosomy Yp
- partial androgen insensitivity syndrome
- Kallmann syndrome
- isochromosomy Yq
- 46,XX ovotesticular disorder of sex development
- spermatogenic failure 63
- ring chromosome Y
- 46,XY disorder of sex development due to 5-alpha-reductase 2 deficiency
