SOHLH2
Description
The SOHLH2 (spermatogenesis and oogenesis specific basic helix-loop-helix 2) is a protein-coding gene located on chromosome 13.
SOHLH2 is also known as SOSF2, SPATA28, TEB1, bHLHe81.
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
- spinocerebellar ataxia type 32
- isochromosomy Yp
- 46,XX testicular disorder of sex development
- spermatogenic failure 63
- isochromosomy Yq
- spermatogenic failure 61
- spermatogenic failure 74
- spermatogenic failure 73
- spermatogenic failure 48
- congenital bilateral absence of vas deferens
- ring chromosome Y
- spermatogenic failure 72
