LONP1 wt Allele

Preferred Label : LONP1 wt Allele;

NCIt synonyms : Protease, Serine, 15 Gene; LonHS; Lon Peptidase 1, Mitochondrial wt Allele; PIM1; hLON; Lon, E. coli, Homolog of Gene; LONP; PRSS15; CODASS; LON;

NCIt definition : Human LONP1 wild-type allele is located in the vicinity of 19p13.2 and is approximately 29 kb in length. This allele, which encodes Lon protease homolog, mitochondrial protein, plays a role in selective proteolysis of damaged polypeptides, misfolded proteins and short-lived regulatory proteins. Mutation of the gene is associated with CODAS syndrome.;

GenBank Accession Number : U02389;

Details

Origin ID

C202941;

OMIM relation
- Lon peptidase 1, mitochondrial [OMIM gene]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 19p13.2 [NCIt concept]
gene_plays_role_in_process
- ATP Hydrolysis [NCIt concept]
- DNA Binding [NCIt concept]
- Hydrolysis [NCIt concept]
- Protein Degradation Process [NCIt concept]
- Proteolysis [NCIt concept]
- RNA Binding [NCIt concept]
- Unfolded Protein Response [NCIt concept]

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