MRPS12 Products

Description

MRPS12, also known as Mitochondrial Ribosomal Protein S12, consists of a 138 amino acid isoform that is 15 kDa, and is involved in the synthesis of proteins within the mitochondria, though its specific purpose is unknown. MRPS12 is currently being used in research with several diseases and disorders, such as autosomal dominant nonsyndromic deafness, esophageal carcinoma, mycobacterium tuberculosis, esophagitis, pneumonia, carcinoma, malaria, and sensorineural hearing loss, to determine its relationship with each condition. MRPS12 interacts with SPINK7, C14orf1, UNC119, CRMP1, and LRIF1 during the process of translation.(provided by RefSeq)

Bioinformatics

Entrez	6183 Human
Uniprot	NP_203526 Human AAH01617 Human NM_021107 Human O15235 Human NP_066930 Human
Product By Gene ID	6183
Alternate Names	ribosomal protein, mitochondrial, S12 MT-RPS12 MPR-S12 MRP-S12 28S ribosomal protein S12, mitochondrial RPS12 RPSM12S12mt RPMS12 mitochondrial ribosomal protein S12

Diseases related to MRPS12

Discover more about diseases related to MRPS12.

Melas Syndrome
Osteosarcoma
Metabolic Diseases
Hereditary Diseases
Neuromuscular Diseases
Meniere Disease
Merrf Syndrome

Pathways for MRPS12

View related products by pathway and learn more about each of the pathways below.

Cell Proliferation
Translation
Aging
Oxidative Phosphorylation
Localization

PTMs for MRPS12

Learn more about PTMs related to MRPS12.

Phosphorylation

Bioinformatics Tool for MRPS12

Discover related pathways, diseases and genes to MRPS12. Need help? Read the Bioinformatics Tool Guide for instructions on using this tool.