Homo sapiens Gene: TSPYL1
Summary
InnateDB Gene IDBG-95651.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol TSPYL1
Gene Name TSPY-like 1
Synonyms TSPYL
Species Homo sapiens
Ensembl Gene ENSG00000189241
Encoded Proteins
TSPY-like 1
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
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]
Gene Information
Type Protein coding
Genomic Location Chromosome 6:116276578-116279903
Strand Reverse strand
Band q22.1
Transcripts
ENST00000368608 ENSP00000357597
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 9 experimentally validated interaction(s) in this database.
Experimentally validated
Total 9 [view]
Protein-Protein 9 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0019899 enzyme binding
Biological Process
GO:0006334 nucleosome assembly
GO:0008150 biological_process
Cellular Component
GO:0005634 nucleus
GO:0005730 nucleolus
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt Q9H0U9
TrEMBL
UniProt Splice Variant
Entrez Gene 7259
UniGene Hs.458358 Hs.743377
RefSeq NM_003309
HUGO HGNC:12382
OMIM 604714
CCDS CCDS34518
HPRD
IMGT
EMBL AF042181 AL050331 AL136629 BC048969 CH471051
GenPept AAC62384 AAH48969 CAB55883 CAB66564 EAW48232
RNA Seq Atlas 7259