TSPYL1( Human )

Entrez Gene 7259 Entrez Gene 7259
TSPY like 1

Alias

TSPYL

The protein encoded by this gene is found in the nucleolus and is similar to that of a family of genes on the Y-chromosome. This gene is intronless. Defects in this gene are a cause of sudden infant death with dysgenesis of the testes syndrome (SIDDT). [provided by RefSeq, Dec 2009].

Product Category