RPL5
Sign in to saveAlso known as DBA6, L5, PPP1R135, MSTP030, Ribosomal protein L5, uL18
protein-coding gene in the species Homo sapiens
In the Vinony graph
Vinony's link graph records 219 inbound references to RPL5, and connects out to PubMed, protein biosynthesis and translation.
Vinony files it under Genes on human chromosome 1 and Ribosomal proteins.
Vinony links it to 6 Wikipedia language editions.
Gene data
RPL5- Name
- ribosomal protein L5
- Type
- protein-coding
- Position
- 92,831,990–92,841,924 (+)
- Aliases
- L5, MSTP030, PPP1R135, uL18
- Ensembl
- ENSG00000122406
- RefSeq RNA
- NM_000969.5, NR_146333.1
- RefSeq protein
- NP_000960.2
Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of four RNA species and approximately 80 structurally distinct proteins. This gene encodes a member of the L18P family of ribosomal proteins and component of the 60S subunit. The encoded protein binds 5S rRNA to form a stable complex called the 5S ribonucleoprotein particle (RNP), which is necessary for the transport of nonribosome-associated cytoplasmic 5S rRNA to the nucleolus for assembly into ribosomes. The encoded protein may also function to inhibit tumorigenesis through the activation of downstream tumor suppressors and the downregulation of oncoprotein expression. Mutations in this gene have been identified in patients with Diamond-Blackfan Anemia (DBA). This gene is co-transcribed with the small nucleolar RNA gene U21, which is located in its fifth intron. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed throughout the genome. [provided by RefSeq, Mar 2017].
Gene Ontology
Biological process
Molecular function
Pathways
via MyGene.info
Gene · Ensembl
ribosomal protein L5
- Symbol
- RPL5
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 1:92,831,990-92,841,924
- Strand
- Forward (+)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
Show 8 more facts
- HomoloGene ID
- 110649
- genomic start
- 93297582
- found in taxon
- Homo sapiens
- exact match
- identifiers.org/ncbigene/6125
- cytogenetic location
- 1p22.1
- chromosome
- human chromosome 1
- genomic end
- 93307481
- genetic association
- Diamond-Blackfan anemia
via Wikidata · CC0