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GENE INFORMATION

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Gene name

TSPYL1 (HGNC Symbol)

Synonyms

TSPYL

Description

TSPY-like 1 (HGNC Symbol)

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]

Chromosome

6 (Chromosome progress)

Cytoband

q22.1

Chromosome location (bp)

116597741 - 116601066

Ensembl

ENSG00000189241 (version 69.37)

Entrez gene

7259

UniProt

Q9H0U9

neXtProt

NX_Q9H0U9

Antibodypedia

TSPYL1 antibodies
 

PROTEIN VIEW

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TSPYL1-001
 
 
 
 
 

PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

TSPYL1-001 ENSP00000357597
ENST00000368608
Q9H0U9
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