Entity Details

Primary name RS23_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionP62266
EntryNameRS23_HUMAN
FullName40S ribosomal protein S23
TaxID9606
Evidenceevidence at protein level
Length143
SequenceStatuscomplete
DateCreated2004-07-05
DateModified2021-06-02

Ontological Relatives

GenesRPS23

GO terms

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GOName
GO:0000184 nuclear-transcribed mRNA catabolic process, nonsense-mediated decay
GO:0002181 cytoplasmic translation
GO:0003723 RNA binding
GO:0003735 structural constituent of ribosome
GO:0005654 nucleoplasm
GO:0005783 endoplasmic reticulum
GO:0005791 rough endoplasmic reticulum
GO:0005829 cytosol
GO:0005840 ribosome
GO:0006412 translation
GO:0006413 translational initiation
GO:0006614 SRP-dependent cotranslational protein targeting to membrane
GO:0016020 membrane
GO:0019083 viral transcription
GO:0022626 cytosolic ribosome
GO:0022627 cytosolic small ribosomal subunit
GO:0034063 stress granule assembly
GO:0042788 polysomal ribosome
GO:1990145 maintenance of translational fidelity

Subcellular Location

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Subcellular Location
Cytoplasm
Rough endoplasmic reticulum

Domains

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DomainNameCategoryType
IPR005680 Ribosomal protein S23, eukaryotic/archaealFamilyFamily
IPR006032 Ribosomal protein S12/S23FamilyFamily
IPR012340 Nucleic acid-binding, OB-foldFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
617412 OMIMBrachycephaly, trichomegaly, and developmental delay (BTDD)An autosomal dominant developmental disorder characterized by brachycephaly, ciliary trichomegaly, dysmorphic features of the face and hands, hearing loss, and developmental delay with short stature. Intellectual disability and autism spectrum disorder may be present in some patients. The disease is caused by variants affecting the gene represented in this entry.