Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
6208
Gene name Gene Name - the full gene name approved by the HGNC.
Ribosomal protein S14
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
RPS14
Synonyms (NCBI Gene) Gene synonyms aliases
EMTB, S14, uS11
Chromosome Chromosome number
5
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
5q33.1
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
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 information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000028 Process Ribosomal small subunit assembly IBA 21873635
GO:0000028 Process Ribosomal small subunit assembly IMP 9152021
GO:0000028 Process Ribosomal small subunit assembly ISS
GO:0000122 Process Negative regulation of transcription by RNA polymerase II IDA 7867928
GO:0000184 Process Nuclear-transcribed mRNA catabolic process, nonsense-mediated decay TAS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
130620 10387 ENSG00000164587
Protein
UniProt ID 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 information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Anemia Anemia, Macrocytic rs118204044, rs118204045, rs118204046, rs121918330, rs869320719, rs869312029, rs121918332, rs869320724, rs767094129, rs786205058, rs786205059, rs137853119, rs137853120, rs137853121, rs1384933966
View all (89 more)
Carcinoma Carcinoma, Carcinoma, Spindle-Cell, Undifferentiated carcinoma rs121912654, rs555607708, rs786202962, rs1564055259 16316942
Leukemia Leukemia, Myelocytic, Acute rs121909646, rs121913488, rs587776834, rs752746786, rs869312821, rs767454740, rs1554564297
Myelodysplasia Myelodysplasia rs141601766, rs1261178797
Associations from Text Mining
Disease Name Relationship Type References
Alzheimer Disease Associate 35766008
Anemia Associate 23943650
Anemia Diamond Blackfan Associate 18202658, 23943650, 32327500
Anemia Macrocytic Associate 31540902
Breast Neoplasms Associate 29081411, 33305312
Carcinoma Hepatocellular Associate 32627011
Carcinoma Squamous Cell Associate 24457517
Chromosome 5q Deletion Syndrome Associate 17916100, 18202658, 18477045, 20378560, 22391559, 23943650, 32327500
Colorectal Neoplasms Associate 35127345
Delayed Cranial Ossification due to CBFB Haploinsufficiency Associate 35617825