MeSH Browser

MeSH Supplementary: apolipoprotein C-II (Toronto)
Unique ID: C050929
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C050929
Entry Term(s): apo C-II, Toronto; apoC-II (Toronto); apolipoprotein C-II, Toronto; apolipoprotein C-IIToronto
Registry Numbers: 107497-50-7
Heading Mapped to: *Apolipoprotein C-II
Frequency: 4
Note: a nonfunctional human mutant apoC-II identified in Toronto; involves a nucleotide deletion in the codon for either Thr68 or Asp69 and a translation reading frame shift; caused apoC-II deficiency
Source: Proc Natl Acad Sci USA 1987;84(1):270
Date of Entry: 1987/02/17
Revision Date: 2006/08/04

Concept UI: M0145187
Registry Numbers: 107497-50-7
Terms: apolipoprotein C-II (Toronto) Preferred Term
Term UI T175192
Date01/01/1955
LexicalTag NON
ThesaurusID NLM (1987); apo C-II, Toronto
Term UI T661043
Date12/05/2005
LexicalTag NON
ThesaurusID NLM (2005); apoC-II (Toronto)
Term UI T175191
Date01/01/1955
LexicalTag NON
ThesaurusID NLM (1987); apolipoprotein C-II, Toronto
Term UI T661040
Date12/05/2005
LexicalTag NON
ThesaurusID NLM (2005); apolipoprotein C-IIToronto
Term UI T661041
Date12/05/2005
LexicalTag NON
ThesaurusID NLM (2005)

apolipoprotein C-II (Toronto) MeSH Supplementary Concept Data 2025