MRPL3 Gene Summary [Human]

Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein that belongs to the L3P ribosomal protein family. A pseudogene corresponding to this gene is found on chromosome 13q. [provided by RefSeq, Jul 2008]

Details

Type
Protein Coding
Official Symbol
MRPL3
Official Name
mitochondrial ribosomal protein L3 [Source:HGNC Symbol;Acc:HGNC:10379]
Ensembl ID
ENSG00000114686
Bio databases IDs NCBI: 11222 Ensembl: ENSG00000114686
Aliases mitochondrial ribosomal protein L3
Synonyms 2010320L16Rik, 5930422H18Rik, COXPD9, dcr, L3mt, mitochondrial ribosomal protein L3, MRL3, RPML3, uL3m
Species
Human, Homo sapiens
OrthologiesMouseRat

Protein Domains

A protein domain is a distinct structural or functional region within a protein that can evolve, function, and exist independently of the rest of the protein chain. These domains in human MRPL3 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
  • Ribosomal protein L3
  • structural constituent of ribosome
  • rpl3p
  • RNA binding

Top Findings

The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
regulated by
disease
  • bipolar disorder
  • neonatal encephalopathy
  • combined oxidative phosphorylation deficiency 9
  • mitochondrial disorder
phenotypes
  • Combined oxidative phosphorylation defect type 9
  • COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 9

Subcellular Expression

Locations within the cell where the protein is known or predicted to be active, providing insight into its function and cellular context.
  • Cytoplasm
  • ribosome
  • Mitochondria
  • mitochondrial inner membrane

Gene Ontology Annotations

Describes the biological processes, cellular components, and molecular functions associated with the human MRPL3 gene, providing context for its role in the cell.

Biological Process

Functions and activities the gene product is involved in
  • mitochondrial translation
  • translation

Cellular Component

Where in the cell the gene product is active
  • mitochondrion
  • mitochondrial large ribosomal subunit
  • mitochondrial inner membrane

Molecular Function

What the gene product does at the molecular level
  • RNA binding
  • structural constituent of ribosome

Gene-Specific Assays for Results You Can Trust

Streamline your workflow with assays designed for this gene. Our targeted dPCR and qPCR assays help you generate meaningful data – efficiently and accurately.