SCML2
Description
The SCML2 (Scm polycomb group protein like 2) is a protein-coding gene located on chromosome X.
SCML2 is a protein that is thought to be part of the Polycomb group (PcG) of proteins. PcG proteins work together in large groups to keep certain genes turned off, especially genes that control how a body develops (called homeotic genes). This helps make sure that the right genes are switched on at the right time during development.
SCML2 is also known as -.
Associated Diseases
- partial chromosome Y deletion
- male infertility with teratozoospermia due to single gene mutation
- spermatogenic failure, X-linked, 2
- spermatogenic failures 50
- spermatogenic failure 25
- spermatogenic failure 61
- spermatogenic failure 73
- spermatogenic failure 74
- spermatogenic failure 48
- isochromosomy Yp
- spermatogenic failure 63
- congenital bilateral absence of vas deferens
- spermatogenic failure 22
- spermatogenic failure 70
- spermatogenic failure 52
- spermatogenic failure 23
- spinocerebellar ataxia type 32
- 46,XX testicular disorder of sex development
- spermatogenic failure 29