CHST8
Description
The CHST8 (carbohydrate sulfotransferase 8) is a protein-coding gene located on chromosome 19.
CHST8 is also known as GALNAC4ST1, GalNAc4ST, PSS3.
Associated Diseases
- peeling skin syndrome type A
- peeling skin syndrome
- isolated congenital hypogonadotropic hypogonadism
- Kallmann syndrome
- partial androgen insensitivity syndrome
- 46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome
- congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency
- hypogonadotropic hypogonadism
- Perrault syndrome
- 46,XY complete gonadal dysgenesis
- 46,XX testicular disorder of sex development
- obesity due to congenital leptin deficiency
- hypergonadotropic hypogonadism-cataract syndrome
- congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency
- Leydig cell hypoplasia
