| RPS4X | 
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| Identifiers | 
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| Aliases | RPS4X, CCG2, DXS306, RPS4, S4, SCAR, SCR10, ribosomal protein S4, X-linked, ribosomal protein S4 X-linked | 
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| External IDs | OMIM: 312760; MGI: 98158; HomoloGene: 90857; GeneCards: RPS4X; OMA:RPS4X - orthologs | 
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| | Gene location (Mouse) | 
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 |  |  | Chr. | X chromosome (mouse) | 
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 |  |  | Band | X D|X 45.2 cM | Start | 101,228,547 bp | 
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 | End | 101,233,000 bp | 
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| Wikidata | 
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40S ribosomal protein S4, X isoform is a protein that in humans is encoded by the RPS4X gene.
Ribosomes, organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes ribosomal protein S4, a component of the 40S subunit. Ribosomal protein S4 is the only ribosomal protein known to be encoded by more than one gene, namely this gene and ribosomal protein S4, Y-linked (RPS4Y). The 2 isoforms encoded by these genes are not identical, but are functionally equivalent. Ribosomal protein S4 belongs to the S4E family of ribosomal proteins. This gene is not subject to X-inactivation. It has been suggested that haploinsufficiency of the ribosomal protein S4 genes plays a role in Turner syndrome; however, this hypothesis is controversial. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome.