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7259
TSPYL1 TSPY like 1 [ Homo sapiens (human) ]
Source: NCBI Gene (ID 7259)
Symbol: TSPYL1
Full name: TSPY like 1
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Also known as: TSPYL
Summary: 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]
Orthologs: mouse
Gene size: 5073bp
Exon count: 1