TSPYL1 Back

TSPY-like 1

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NCBI Description of TSPYL1

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). Sequence Note: The RefSeq transcript and protein were derived from genomic sequence to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on alignments.

Community Annotation of TSPYL1 Add / Edit TSPYL1: Annotations

No community annotations yet for TSPYL1.
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Figure notes


• "Mouse over" a mutation to see details.
• Missense green saturation indicates evolutionary conservation of the mutated positions.
• Red hashes in protein strip are splice sites.
• Blue-white-red bars are log2 copy ratio distributions (–1 to +1) from Zack et al. (2013).


Legend

TSPYL1 is highly significantly mutated in
(none)
TSPYL1 is significantly mutated in
(none)
TSPYL1 is near significance in
(none)

Click on a tumor type to see its full list of significant genes.

Data details


Mutation list for TSPYL1