LONP1 Chromosome 19

Lon peptidase 1, mitochondrial
105 variants 105 Health Risk

Upload your DNA to see your personal genotypes for variants in LONP1.

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
RS1025252513 Health Risk Conflicting classifications of pathogenicity
RS112807920 Health Risk Conflicting classifications of pathogenicity LONP1-related disorder, LONP1-related disorder
RS116591583 Health Risk Conflicting classifications of pathogenicity LONP1-related disorder, LONP1-related disorder
RS1319441126 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1382601981 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS138631909 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS139555567 Health Risk Conflicting classifications of pathogenicity LONP1-related disorder, LONP1-related disorder
RS139759295 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS139791767 Health Risk Conflicting classifications of pathogenicity CODAS syndrome, Inborn genetic diseases, CODAS syndrome
RS140317309 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS141593936 Health Risk Conflicting classifications of pathogenicity CODAS syndrome, Inborn genetic diseases, CODAS syndrome
RS141916070 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS142068825 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS143983421 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS144822855 Health Risk Conflicting classifications of pathogenicity CODAS syndrome, CODAS syndrome
RS145519500 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, CODAS syndrome, LONP1-related disorder
RS146515571 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS147029972 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS147307965 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS147591431 Health Risk Conflicting classifications of pathogenicity CODAS syndrome, Inborn genetic diseases, CODAS syndrome
RS148214998 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS149169865 Health Risk Conflicting classifications of pathogenicity LONP1-related disorder, LONP1-related disorder
RS149596661 Health Risk Conflicting classifications of pathogenicity CODAS syndrome, Inborn genetic diseases, CODAS syndrome
RS149844957 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS150100006 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS150732086 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, CODAS syndrome, Inborn genetic diseases
RS186834921 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS199803800 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS200317240 Health Risk Conflicting classifications of pathogenicity CODAS syndrome, Inborn genetic diseases, LONP1-related disorder
RS200551277 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS200636537 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS201187879 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS201664019 Health Risk Conflicting classifications of pathogenicity See cases, CODAS syndrome, See cases
RS201679198 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS368178461 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS368654972 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS368898285 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS370434508 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS371606894 Health Risk Conflicting classifications of pathogenicity CODAS syndrome, CODAS syndrome
RS371793819 Health Risk Conflicting classifications of pathogenicity CODAS syndrome, CODAS syndrome
RS372205884 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS373028270 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS373094123 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS373182816 Health Risk Conflicting classifications of pathogenicity CODAS syndrome, LONP1-related disorder, CODAS syndrome
RS373284466 Health Risk Conflicting classifications of pathogenicity CODAS syndrome, Inborn genetic diseases, CODAS syndrome
RS373597948 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS373661439 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS374091667 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS374217265 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, CODAS syndrome, Inborn genetic diseases
RS375486513 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
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