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TSPYL1

Official Full Name
TSPY like 1
Organism
Homo sapiens
GeneID
7259
Background
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]
Synonyms
TSPYL;

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