LONP1 Chromosome 19

Lon peptidase 1, mitochondrial
105 variants 105 Health Risk

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What This Gene Does
This gene encodes a mitochondrial matrix protein that belongs to the Lon family of ATP-dependent proteases. This protein mediates the selective degradation of misfolded, unassembled or oxidatively damaged polypeptides in the mitochondrial matrix. It may also have a chaperone function in the assembly of inner membrane protein complexes, and participate in the regulation of mitochondrial gene expression and maintenance of the integrity of the mitochondrial genome. Decreased expression of this gene has been noted in a patient with hereditary spastic paraplegia (PMID:18378094). Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Feb 2013]
Gene Info
Gene Group
"AAA ATPases|Serine proteases|Mitochondrial nucleoid associated proteins"
Locus Type
gene with protein product
Location
19p13.2
Ensembl
ENSG00000196365
Associated Conditions (14)
LONP1-related disorder
Inborn genetic diseases
CODAS syndrome
See cases
Neurodevelopmental disorder
Gastric cancer
Hepatocellular carcinoma
Malignant tumor of esophagus
Malignant lymphoma
large B-cell
diffuse
Thyroid cancer
nonmedullary
1
Key Variants
All Variants (105)
RSID Category Clinical Significance Conditions
RS2512415212 Health Risk Pathogenic See cases, See cases
RS2512443872 Health Risk Pathogenic
RS730880293 Health Risk Pathogenic CODAS syndrome, CODAS syndrome
RS879255248 Health Risk Pathogenic CODAS syndrome, CODAS syndrome
RS879255249 Health Risk Pathogenic CODAS syndrome, CODAS syndrome
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