SPATC1L
Description
The SPATC1L (spermatogenesis and centriole associated 1 like) is a protein-coding gene located on chromosome 21.
SPATC1L is a protein encoded by the SPATC1L gene in humans. This gene's location and details can be found in the UCSC Genome Browser.
SPATC1L is also known as C21orf56.
Associated Diseases
- male infertility with teratozoospermia due to single gene mutation
- spermatogenic failure 20
- spermatogenic failure 5
- spermatogenic failure 72
- spermatogenic failure 26
- spermatogenic failure 31
- spermatogenic failure 27
- spermatogenic failure 46
- spermatogenic failure 18
- spermatogenic failure 43
- spermatogenic failure 19
- spermatogenic failure 49
- spermatogenic failure 45
- spermatogenic failure 42
- spermatogenic failure, X-linked, 3
- spermatogenic failure 40
- partial chromosome Y deletion
- spermatogenic failure 39