MRPL19 Products

Description

Belonging to the ribosomal protein L19P family, MRPL19 plays an important role in cell translation. These Mammalian mitochondrial ribosomal proteins contain a small 28S subunit and a large 39S subunit, and consist of 75% protein to rRNA composition. The ribosomal proteins also help in protein synthesis within the mitochondrion. This gene also acts as a structural component of mitochondrial ribosomes, and encodes the 39S subunit protein. Interacting proteins include SMURF2, TRIM63, MAGEC1, MRPL12 and MRPL11. Dyslexia is also a common disease associated with the MRPL19 gene.

Bioinformatics

Entrez	9801 Human
Uniprot	P49406 Human AAH30144 Human NP_055578 Human
Product By Gene ID	9801
Alternate Names	mitochondrial RPML15 MGC20675 RLX1 MRPL1539S ribosomal protein L19, mitochondrial MRP-L15MRP-L19 KIAA0104L19mt L15mt mitochondrial ribosomal protein L19

Diseases related to MRPL19

Discover more about diseases related to MRPL19.

Dyslexia
Malignant Neoplasms
Neoplasms
Mammary Neoplasms
Malignant Neoplasm Of Breast
Language Disorders
Specific Language Impairment
Dysequilibrium Syndrome
Non-neoplastic Disorder
Developmental Reading Disorder
Language Development Disorders
Malignant Paraganglionic Neoplasm
Carcinoma
Colorectal Neoplasms
Pancreatic Neoplasm
Leukemia
Lymphoid Leukemia
Malignant Neoplasm Of Pancreas
Colorectal Cancer
Chronic Lymphocytic Leukemia

Pathways for MRPL19

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

Reverse Transcription
Cognition

Bioinformatics Tool for MRPL19

Discover related pathways, diseases and genes to MRPL19. Need help? Read the Bioinformatics Tool Guide for instructions on using this tool.