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2024年12月25日 · RPS18 (Ribosomal Protein S18) is a Protein Coding gene. Diseases associated with RPS18 include Diamond-Blackfan Anemia. Among its related pathways are Peptide chain elongation and Nervous system development. Gene Ontology (GO) annotations related to this gene include nucleic acid binding and RNA binding.

2025年1月4日 · Ribosomes, the 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 a ribosomal protein that is a component of the 40S subunit.

We now provide the "Disease & Variants" viewer in its own tab. The viewer provides 83 variants from UniProt as well as other sources including ClinVar and dbSNP. Go to variant viewer. Showing features for initiator methionine, modified residue, modified residue (large scale data), chain, cross-link. Component of the small ribosomal subunit. Search…

Ribosomal protein S18e seems to act as a molecular staple fixing the 18S rRNA 3'-major domain core. Observational study of gene-disease association. (HuGE Navigator) Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit.

2025年2月9日 · Ribosomal protein S18 identified as a cofilin-binding protein by using phage display library. Identification of genes overexpressed in tumors through preferential expression screening in trophoblasts.

ribosomal protein S18 [Source:HGNC Symbol;Acc: 10401] D6S218E, HKE3, KE-3, KE3, S18. Chromosome 6: 33,239,787-33,244,287 forward strand. GRCh37:CM000668.1. View alleles of this gene on alternative sequences. This gene has 8 transcripts (splice variants) and 1 gene allele. Show transcript table.

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Ribosomal protein S18, also known as RPS18, is a human gene. [1] Ribosomes, the 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 …

View mouse Rps18 Chr17:34170972-34174639 with: phenotypes, sequences, polymorphisms, proteins, references, function, expression