1. Gene
  2. MRPS25 - mitochondrial ribosomal protein S25 Gene

MRPS25 - mitochondrial ribosomal protein S25 Gene

Homo sapiens

Also known as RPMS25; COXPD50; MRP-S25

Gene ID: 64432 | Gene type: protein coding

About MRPS25

Cytogenetic location: 3p25.1 Genomic coordinates (GRCh38): 3:15,042,251-15,065,315 (from NCBI)

This gene has 32 transcripts (splice variants), 195 orthologues and is associated with 1 phenotype. Ubiquitous expression in brain (RPKM 11.7), thyroid (RPKM 11.6) and 25 other tissues.

Summary

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 28S subunit protein. A pseudogene corresponding to this gene is found on chromosome 4. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]

MRPS25 Products(1)

mRNA Protein Name
NM_022497.5 NP_071942.1 28S ribosomal protein S25, mitochondrial

MRPS25 Protein Structure

L51_S25_CI-B8

L51_S25_CI-B8: Mitochondrial ribosomal protein L51 / S25 / CI-B8 domain (44 - 94)

  • 0
  • 100
  • 173 a.a.
Protein Preferred Names Protein Names

28S ribosomal protein S25, mitochondrial

S25mt

Related Diseases

Diseases Alias
Combined Oxidative Phosphorylation Deficiency 50

COXPD50

Dyskinetic Cerebral Palsy

Athetoid Cerebral Palsy

Athetoid Dyskinetic Cerebral Palsy

Cerebral Palsy Athetoid

Cerebral Palsy Dyskinetic

Athetoid Cerebral Paralysis

Dyskinetic Cerebral Paralysis

Vogt Disease

Athetoid Cerebrum Palsy

Double Athetosis Syndrome

État Marbré

Mitochondrial Encephalomyopathy

Mitochondrial Encephalomyopathies

Encephalomyopathy, Mitochondrial

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Rattus norvegicus MRPS25 RGD RGD:1308770
Mus musculus MRPS25 MGD MGI:1928140
Felis catus MRPS25 VGNC VGNC:63620
Bos taurus MRPS25 VGNC VGNC:31665
Macaca mulatta MRPS25 VGNC VGNC:74764
Canis familiaris MRPS25 VGNC VGNC:43416