| Gene Symbol | TSPYL1 |
| Entrez Gene ID | 7259 |
| Full Name | TSPY like 1 |
| Synonyms | TSPYL |
| General protein information |
|
| Gene Type | protein-coding |
| Organism | Homo sapiens(human) |
| Genome | |
| 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]. |
| Disorder MIM: | |
| Disorder Html: | Sudden infant death with dysgenesis of the testes syndrome, 608800 (3) |








































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