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).
TSPYL1; TSPY-like 1; TSPY like , TSPYL; testis-specific Y-encoded-like protein 1; SIDDT; Testis specific like protein Y encoded; Testis specific Y encoded like protein 1; TSPY like; TSPY like 1; TSPY like protein 1; TSPYL; OTTHUMP00000017052; TSPY-like protein 1; testis-specific-like protein, Y encoded
TSPYL1 involved in several pathways and played different roles in them. We selected most pathways TSPYL1 participated on our site, such as SIDS Susceptibility Pathways, which may be useful for your reference. Also, other proteins which involved in the same pathway with TSPYL1 were listed below. Creative Biomart supplied nearly all the proteins listed, you can search them on our site.
TSPYL1 has several biochemical functions, for example, enzyme binding. Some of the functions are cooperated with other proteins, some of the functions could acted by TSPYL1 itself. We selected most functions TSPYL1 had, and list some proteins which have the same functions with TSPYL1. You can find most of the proteins on our site.
Function enzyme binding
Related Protein HMGA1-RS1; NOTCH3; HIST1H2AN; HNRNPUL1; LYN; CUTA; RPS3; UGT1A4; HDAC2; JUN
TSPYL1 has direct interactions with proteins and molecules. Those interactions were detected by several methods such as yeast two hybrid, co-IP, pull-down and so on. We selected proteins and molecules interacted with TSPYL1 here. Most of them are supplied by our site. Hope this information will be useful for your research of TSPYL1.