Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
6224
Gene name Gene Name - the full gene name approved by the HGNC.
Ribosomal protein S20
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
RPS20
Synonyms (NCBI Gene) Gene synonyms aliases
S20, uS10
Chromosome Chromosome number
8
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
8q12.1
Summary Summary of gene provided in NCBI Entrez Gene.
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 pro
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT439734 hsa-miR-155-5p HITS-CLIP 22473208
MIRT439734 hsa-miR-155-5p HITS-CLIP 22473208
MIRT1317754 hsa-miR-4670-3p CLIP-seq
MIRT1317755 hsa-miR-548aa CLIP-seq
MIRT1317756 hsa-miR-548ac CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0002181 Process Cytoplasmic translation IC 23636399
GO:0002181 Process Cytoplasmic translation NAS 25901680
GO:0003723 Function RNA binding HDA 22658674, 22681889
GO:0003723 Function RNA binding IEA
GO:0003735 Function Structural constituent of ribosome HDA 15883184
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
603682 10405 ENSG00000008988
Protein
UniProt ID P60866
Protein name Small ribosomal subunit protein uS10 (40S ribosomal protein S20)
Protein function Component of the small ribosomal subunit (PubMed:23636399). The ribosome is a large ribonucleoprotein complex responsible for the synthesis of proteins in the cell (PubMed:23636399).
PDB 4UG0 , 4V6X , 5A2Q , 5AJ0 , 5FLX , 5LKS , 5OA3 , 5T2C , 5VYC , 6FEC , 6G51 , 6G53 , 6G5H , 6G5I , 6IP5 , 6IP6 , 6IP8 , 6OLE , 6OLF , 6OLG , 6OLI , 6OLZ , 6OM0 , 6OM7 , 6QZP , 6XA1 , 6Y0G , 6Y2L , 6Y57 , 6YBS , 6Z6L , 6Z6M , 6Z6N , 6ZLW , 6ZM7 , 6ZME , 6ZMI , 6ZMO , 6ZMT , 6ZMW , 6ZN5 , 6ZOJ , 6ZOL , 6ZON , 6ZP4 , 6ZUO , 6ZV6 , 6ZVH , 6ZVJ , 6ZXD , 6ZXE
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00338 Ribosomal_S10 21 115 Ribosomal protein S10p/S20e Family
Sequence
Sequence length 119
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Ribosome
Coronavirus disease - COVID-19
  L13a-mediated translational silencing of Ceruloplasmin expression
SRP-dependent cotranslational protein targeting to membrane
Viral mRNA Translation
Major pathway of rRNA processing in the nucleolus and cytosol
Translation initiation complex formation
Formation of a pool of free 40S subunits
Formation of the ternary complex, and subsequently, the 43S complex
Ribosomal scanning and start codon recognition
GTP hydrolysis and joining of the 60S ribosomal subunit
Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC)
Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC)
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Anemia Diamond-Blackfan anemia N/A N/A GenCC
Colorectal Cancer familial colorectal cancer, familial colorectal cancer type X N/A N/A GenCC
Lynch Syndrome Lynch syndrome N/A N/A GenCC
Systemic lupus erythematosus Systemic lupus erythematosus N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Alzheimer Disease Associate 35766008
Alzheimer Disease Inhibit 36195955
Anemia Diamond Blackfan Associate 32790018
Breast Neoplasms Associate 32444848
Carcinoma Hepatocellular Associate 36378050
Carcinoma Renal Cell Associate 36484407
Colorectal Neoplasms Associate 24941021, 32790018, 35682850
Colorectal Neoplasms Hereditary Nonpolyposis Associate 24941021, 35682850
COVID 19 Associate 36509426
Glioblastoma Associate 21649900, 26506620