CCDC169-SOHLH2
Description
The CCDC169-SOHLH2 (CCDC169-SOHLH2 readthrough) is a protein-coding gene located on chromosome 13.
CCDC169-SOHLH2 is a gene that encodes a protein that plays a role in the development of the nervous system. The protein is thought to be involved in the regulation of neuronal migration and differentiation. It may also be involved in the formation of synapses, the junctions between neurons.
CCDC169-SOHLH2 is a gene that encodes a protein that plays a role in the development of the nervous system. The protein is thought to be involved in the regulation of neuronal migration and differentiation. It may also be involved in the formation of synapses, the junctions between neurons.
CCDC169-SOHLH2 is also known as C13orf38-SOHLH2, SOHLH2, TEB1.
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
- spermatogenic failure 20
- spermatogenic failure 65
- spermatogenic failure, X-linked, 3
- spermatogenic failure 44
