MPV17 Products

Description

MPV17 encodes a mitochondrial inner membrane protein that is implicated in the metabolism of reactive oxygen species. Mutations in this gene have been associated with the hepatocerebral form of mitochondrial DNA depletion syndrome (MDDS). [provided by RefSeq]

Bioinformatics

Entrez	4358 Human 17527 Mouse 360463 Rat
Uniprot	NM_002437 Human NP_002428.1 Human
Product By Gene ID	4358
Alternate Names	protein Mpv17 human homolog of glomerulosclerosis and nephrotic syndrome murine homolog, glomerulosclerosis MpV17 mitochondrial inner membrane protein

Diseases related to MPV17

Discover more about diseases related to MPV17.

Mitochondrial Diseases
Mitochondrial Dna Depletion
Glomerulosclerosis (disorder)
Dysmyelopoietic Syndromes
Kidney Diseases
Focal Glomerulosclerosis
Liver Diseases
Liver Failure
Nephrotic Syndrome
Glomerulonephritis
Sensorineural Hearing Loss (disorder)
Hypoglycemia
Complete Hearing Loss
Hypertensive Disease
External Ophthalmoplegia
Navajo Neurohepatopathy
Ophthalmoplegia
Acidosis
Acidosis, Lactic
Kidney Failure

Pathways for MPV17

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

Oxidative Phosphorylation
Transport
Localization
Electron Transport
Aging
Electron Transport Chain
Programmed Cell Death
Ion Transport
Natriuresis
Dna Replication
Translation
Mitochondrial Genome Maintenance
Cell Death
Cellular Localization
Protein Import
Pathogenesis
Rna Interference

PTMs for MPV17

Learn more about PTMs related to MPV17.

Phosphorylation
Cleavage

Bioinformatics Tool for MPV17

Discover related pathways, diseases and genes to MPV17. Need help? Read the Bioinformatics Tool Guide for instructions on using this tool.