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TSPYL1 GeneTSPY-like 1 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] |
TSPYL1 Gene SetFrom Pathway Commons Protein-Protein Interactions interacting proteins for TSPYL1 from the Pathway Commons Protein-Protein Interactions dataset. |
TSPYL1 Gene SetFrom CM4AI KOLF21J CRISPRi Gene Perturbation Atlas genes differentially expressed following the TSPYL1 gene perturbation from the CM4AI KOLF21J CRISPRi Gene Perturbation Atlas. |
a-TSPYL1 (TSPYL1) Gene Setproteins in the a-TSPYL1 (TSPYL1) protein complex recovered by IP-MS from the NURSA Protein Complexes dataset. |