Gene Gene information from NCBI Gene database.
Entrez ID 6208
Gene name Ribosomal protein S14
Gene symbol RPS14
Synonyms (NCBI Gene)
EMTBS14uS11
Chromosome 5
Chromosome location 5q33.1
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.
106
miRTarBase ID miRNA Experiments Reference
MIRT050273 hsa-miR-25-3p CLASH 23622248
MIRT049275 hsa-miR-92a-3p CLASH 23622248
MIRT044278 hsa-miR-106b-5p CLASH 23622248
MIRT043360 hsa-miR-331-3p CLASH 23622248
MIRT043360 hsa-miR-331-3p CLASH 23622248
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
41
GO ID Ontology Definition Evidence Reference
GO:0000028 Process Ribosomal small subunit assembly IBA
GO:0000028 Process Ribosomal small subunit assembly ISS
GO:0000122 Process Negative regulation of transcription by RNA polymerase II IDA 7867928
GO:0002181 Process Cytoplasmic translation IC 3785212, 8706699, 15883184, 23636399
GO:0002181 Process Cytoplasmic translation IMP 3683397, 9152021
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
130620 10387 ENSG00000164587
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P62263
Protein name Small ribosomal subunit protein uS11 (40S ribosomal protein S14)
Protein function Component of the small ribosomal subunit. The ribosome is a large ribonucleoprotein complex responsible for the synthesis of proteins in the cell. Part of the small subunit (SSU) processome, first precursor of the small eukaryotic ribosomal subu
PDB 4UG0 , 4V6X , 5A2Q , 5AJ0 , 5FLX , 5LKS , 5OA3 , 5T2C , 5VYC , 6FEC , 6G18 , 6G4S , 6G4W , 6G51 , 6G53 , 6G5H , 6G5I , 6IP5 , 6IP6 , 6IP8 , 6OLE , 6OLF , 6OLG , 6OLI , 6OLZ , 6OM0 , 6OM7 , 6QZP , 6XA1 , 6Y0G , 6Y2L , 6Y57 , 6YBD , 6YBW , 6Z6L , 6Z6M , 6Z6N , 6ZLW , 6ZM7 , 6ZME , 6ZMI , 6ZMO , 6ZMT , 6ZMW , 6ZN5 , 6ZOJ , 6ZOK , 6ZON , 6ZP4 , 6ZUO , 6ZV6
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00411 Ribosomal_S11 29 147 Ribosomal protein S11 Family
Sequence
Sequence length 151
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 (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
5
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
CARCINOMA CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CHROMOSOME 5Q DELETION SYNDROME CTD, HPO
CTD, HPO
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
HYPOXIA CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
MYELODYSPLASTIC SYNDROME ASSOCIATED WITH ISOLATED DEL CHROMOSOME ABNORMALITY Orphanet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
5q-syndrome 5q-syndrome BEFREE 17916100, 18202658, 18477045, 19016715, 19322210, 20211165, 20378560, 20491881, 20733155, 20980806, 21068437, 21435510, 21536236, 21873545, 21943668
View all (7 more)
★☆☆☆☆
Found in Text Mining only
5q-syndrome 5q-syndrome ORPHANET_DG 22571696
★☆☆☆☆
Found in Text Mining only
5q-syndrome 5q-syndrome CTD_human_DG
★☆☆☆☆
Found in Text Mining only
5q-syndrome 5q-syndrome GENOMICS_ENGLAND_DG
★☆☆☆☆
Found in Text Mining only
Alzheimer Disease Alzheimer disease Pubtator 35766008 Associate
★☆☆☆☆
Found in Text Mining only
Anaplastic carcinoma Anaplastic Carcinoma CTD_human_DG 16316942
★☆☆☆☆
Found in Text Mining only
Anemia Anemia Pubtator 23943650 Associate
★☆☆☆☆
Found in Text Mining only
Anemia Anemia BEFREE 25645650
★☆☆☆☆
Found in Text Mining only
Anemia Macrocytic Macrocytic anemia Pubtator 31540902 Associate
★☆☆☆☆
Found in Text Mining only
Anemia, Diamond-Blackfan Anemia BEFREE 18202658, 21068437, 21130407, 22734070, 23943650
★☆☆☆☆
Found in Text Mining only