Gene Gene information from NCBI Gene database.
Entrez ID 6204
Gene name Ribosomal protein S10
Gene symbol RPS10
Synonyms (NCBI Gene)
DBA9S10eS10
Chromosome 6
Chromosome location 6p21.31
Summary 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.
20
miRTarBase ID miRNA Experiments Reference
MIRT052450 hsa-let-7a-5p CLASH 23622248
MIRT050485 hsa-miR-20a-5p CLASH 23622248
MIRT049763 hsa-miR-92a-3p CLASH 23622248
MIRT044184 hsa-miR-99b-5p CLASH 23622248
MIRT041658 hsa-miR-484 CLASH 23622248
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
31
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 IBA
GO:0003735 Function Structural constituent of ribosome HDA 15883184
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
603632 10383 ENSG00000124614
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P46783
Protein name Small ribosomal subunit protein eS10 (40S ribosomal protein S10)
Protein function Component of the 40S 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
PF03501 S10_plectin 3 98 Plectin/S10 domain Domain
Sequence
MLMPKKNRIAIYELLFKEGVMVAKKDVHMPKHPELADKNVPNLHVMKAMQSLKSRGYVKE
QFAWRHFYWYLTNEGIQYLRDYLHLPPEIVPATLRRSR
PETGRPRPKGLEGERPARLTRG
EADRDTYRRSAVPPGADKKAEAGAGSATEFQFRGGFGRGRGQPPQ
Sequence length 165
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)
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
150
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Diamond-Blackfan anemia Pathogenic; Likely pathogenic rs2113806114, rs2533030608, rs267607022, rs1581931439, rs1765648528 RCV001381292
RCV002428903
RCV001851701
RCV000809206
RCV001035752
Diamond-Blackfan anemia 9 Pathogenic rs2533030608, rs267607021, rs1581931541, rs267607022 RCV005252150
RCV000006562
RCV000006563
RCV000006564
RPS10-related disorder Likely pathogenic rs2533019856 RCV003400021
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Alzheimer Disease Associate 30040709
Anemia Diamond Blackfan Associate 20116044, 22262766, 24675553, 25946618
Hereditary Breast and Ovarian Cancer Syndrome Associate 30206415
Lymphoma Large Cell Anaplastic Associate 30206415
Neoplasms Associate 30607635
Neurodegenerative Diseases Associate 30040709
Obesity Associate 26449484
Sarcopenia Associate 35241739