TSPYL1 Products

Description

The protein encoded by the TSPYL1 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)

Bioinformatics

Entrez	7259 Human
Uniprot	NM_003309 Human AAH48969 Human AAH48969.1 Human NP_003300 Human NP_003300.1 Human
Product By Gene ID	7259
Alternate Names	TSPY-like SIDDT TSPY-like protein 1 TSPYLtestis-specific-like protein, Y encoded testis-specific Y-encoded-like protein 1 TSPY-like 1

Diseases related to TSPYL1

Discover more about diseases related to TSPYL1.

Gonadal Dysgenesis
Congenital Abnormality
Male Infertility
Sudden Infant Death Syndrome
Disorders Of Sex Development
Infertility
Azoospermia
Thalassemia
Hemoglobin F Disease
Xy Female
Hereditary Persistence Of Fetal Hemoglobin Thalassemia
Sudden Death
Oligospermia
Dysequilibrium Syndrome

Pathways for TSPYL1

View related products by pathway and learn more about each of the pathways below.

Chromatin Remodeling
Sex Differentiation
Sex Determination
Pathogenesis

Bioinformatics Tool for TSPYL1

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