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The protein encoded by TSPYL1 is found in the nucleolus and is similar to that of a family of genes on the Y-chromosome. Additionally we are shipping TSPYL1 Antibodies (32) and many more products for this protein.
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Results show that mutations and polymorphisms in the TSPYL1 gene were not associated with sudden infant death syndrome in a cohort of 165 deceased Swiss infants.
Mutations in the TSPYL1 gene do not seem to play a major role in the pathogenesis of idiopathic male infertility, and mutation screening of the TSPYL1 gene can currently not be recommended in routine diagnostics of idiopathic male infertility.
The chromatin remodeling factor (show ASH1L Proteins) TSPYL1 had a very similar pattern of expression with an incremental increase in HPFH and decreased expression in deltabeta-thalassemia.
Mutations in TSPYL1 may contribute to anomalies of testicular development/function.
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).
, TSPY-like protein 1
, testis-specific Y-encoded-like protein 1
, testis-specific-like protein, Y encoded