LPA wt Allele - CISMeF

Preferred Label : LPA wt Allele;

NCIt synonyms : Apolipoprotein(a) Gene; AK38; APOA; Lipoprotein, Lp(a) Gene; LP; Lipoprotein(a) wt Allele;

NCIt definition : Human LPA wild-type allele is located within 6q25.3-q26 and is approximately 134 kb in length. This allele, which encodes apolipoprotein(a) protein, plays a role in proteolysis, lipid metabolism and the regulation of thrombolysis. Aberrant expression of the gene is associated with atherosclerosis.;

NCI Metathesaurus CUI : CL538293;

GenBank Accession Number : X06290;

Details

Origin ID

C140117;

UMLS CUI

C4553344;

Automatic exact mappings (from CISMeF team)
- Apolipoprotein A [LOINC component]
- Apolipoprotein gene (substance) [SNOMED CT concept]
- Lipoprotein (a) (substance) [SNOMED CT concept]
- Lipoprotein a [LOINC component]
- O-phosphoserine trna-selenocysteine trna synthase [OMIM gene]
- apolipoproteins a [MeSH Descriptor]
- lateral pallium [UBERON concept]
- lateral posterior nucleus of thalamus [UBERON concept]
- lower premolar tooth [UBERON concept]
OMIM relation
- Apolipoprotein(a) [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_plays_role_in_process
- Enzyme Inhibition [NCIt concept]
- Hydrolysis [NCIt concept]
- Lipid Metabolic Process [NCIt concept]
- Proteolysis [NCIt concept]
- Proteolytic Processing [NCIt concept]
- Regulation of Proteolysis [NCIt concept]

Keyword's position in hierarchy(ies) :

Main resources

You can consult :

recommendations
documents concerning education
documents for patients