Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
9349
Gene name Gene Name - the full gene name approved by the HGNC.
Ribosomal protein L23
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
RPL23
Synonyms (NCBI Gene) Gene synonyms aliases
L23, rpL17, uL14
Chromosome Chromosome number
17
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
17q12
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
MIRT022730 hsa-miR-124-3p Microarray 18668037
MIRT047046 hsa-miR-183-5p CLASH 23622248
MIRT041095 hsa-miR-503-5p CLASH 23622248
MIRT041095 hsa-miR-503-5p CLASH 23622248
MIRT039746 hsa-miR-615-3p CLASH 23622248
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000122 Process Negative regulation of transcription by RNA polymerase II IMP 19160485
GO:0000184 Process Nuclear-transcribed mRNA catabolic process, nonsense-mediated decay TAS
GO:0001223 Function Transcription coactivator binding IPI 19160485
GO:0003723 Function RNA binding HDA 22658674
GO:0003735 Function Structural constituent of ribosome IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
603662 10316 ENSG00000125691
Protein
UniProt ID P62829
Protein name Large ribosomal subunit protein uL14 (60S ribosomal protein L17) (60S ribosomal protein L23)
Protein function Component of the large ribosomal subunit. The ribosome is a large ribonucleoprotein complex responsible for the synthesis of proteins in the cell.
PDB 4UG0 , 4V6X , 5AJ0 , 5LKS , 5T2C , 6IP5 , 6IP6 , 6IP8 , 6LQM , 6LSR , 6LSS , 6LU8 , 6OLE , 6OLF , 6OLG , 6OLI , 6OLZ , 6OM0 , 6OM7 , 6QZP , 6XA1 , 6Y0G , 6Y2L , 6Y57 , 6Y6X , 6Z6L , 6Z6M , 6Z6N , 6ZM7 , 6ZME , 6ZMI , 6ZMO , 7F5S , 7OW7 , 7XNX , 7XNY , 8A3D , 8FKP , 8FKQ , 8FKR , 8FKS , 8FKT , 8FKU , 8FKV , 8FKW , 8FKX , 8FKY , 8FKZ , 8FL0 , 8FL2 , 8FL3
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00238 Ribosomal_L14 20 140 Ribosomal protein L14p/L23e Domain
Sequence
Sequence length 140
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
Formation of a pool of free 40S subunits
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, Diamond-Blackfan rs118204044, rs118204045, rs118204046, rs121918330, rs869320719, rs869312029, rs121918332, rs869320724, rs767094129, rs786205058, rs786205059, rs137853119, rs137853120, rs137853121, rs1384933966
View all (89 more)
28297620
Unknown
Disease term Disease name Evidence References Source
Alzheimer disease Alzheimer disease GWAS
Associations from Text Mining
Disease Name Relationship Type References
Alzheimer Disease Associate 35766008
Arthritis Reactive Associate 8790600
Atypical Hemolytic Uremic Syndrome Associate 37373158
Colorectal Neoplasms Associate 36341526
HIV Infections Associate 32579550
Infertility Male Associate 36369953
Mucopolysaccharidoses Associate 35456399
Myelodysplastic Syndromes Associate 28539603
Sarcoma Kaposi Associate 40016701
Sertoli Cell Only Syndrome Associate 31603917