Entity Details

Primary name TSYL1_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ9H0U9
EntryNameTSYL1_HUMAN
FullNameTestis-specific Y-encoded-like protein 1
TaxID9606
Evidenceevidence at protein level
Length437
SequenceStatuscomplete
DateCreated2003-08-15
DateModified2021-06-02

Ontological Relatives

GenesTSPYL1

GO terms

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GOName
GO:0000785 chromatin
GO:0003682 chromatin binding
GO:0005634 nucleus
GO:0005654 nucleoplasm
GO:0005730 nucleolus
GO:0006334 nucleosome assembly
GO:0019899 enzyme binding
GO:0042393 histone binding

Subcellular Location

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Subcellular Location
Nucleus

Domains

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DomainNameCategoryType
IPR002164 Nucleosome assembly protein (NAP)FamilyFamily
IPR037231 NAP-like superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
608800 OMIMSudden infant death with dysgenesis of the testes syndrome (SIDDT)Autosomal recessive disorder. Affected infants appear normal at birth, develop signs of visceroautonomic dysfunction early in life, and die before 12 months of age of abrupt cardiorespiratory arrest. Features included bradycardia, hypothermia, severe gastroesophageal reflux, laryngospasm, bronchospasm, and abnormal cardiorespiratory patterns during sleep. Genotypic males with SIDDT had fetal testicular dysgenesis and ambiguous genitalia, with findings such as intraabdominal testes, dysplastic testes, deficient fetal testosterone production, fusion and rugation of the gonadal sac, and partial development of the penile shaft. Female sexual development was normal. Affected infants had an unusual staccato cry, similar to the cry of a goat. The disease is caused by variants affecting the gene represented in this entry.