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Apoc-II), or apolipoprotein C2 is a protein that in humans is encoded by the APOC2 gene. The protein encoded by this gene is secreted in plasma, where it is...
Click to read more »components including apolipoprotein C-II (APOC2) and apolipoprotein E (APOE) to the mature chylomicron. APOC2 is a crucial coenzyme for the activity of...
Click to read more »layer One in 1,000,000 b 207750 Familial apoprotein CII deficiency Altered ApoC2 c 118830 LPL inhibitor in blood Type II a 143890 Familial hypercholesterolemia...
Click to read more »amyloid Semenogelin I Apolipoprotein C2 amyloidosis Apolipoprotein C2 (ApoC2) Apolipoprotein C3 amyloidosis Apolipoprotein C3 (ApoC3) Lect2 amyloidosis...
Click to read more »genes that regulate catabolism of triglyceride-rich lipoproteins (e.g., ApoC2, ApoA5, LMF-1, GPIHBP-1, GPD1) should also be considered.[citation needed]...
Click to read more »human chromosome 19 linkage group FUT1 (H), FUT2 (SE), LE, LU, PEPD, C3, APOC2, D19S7 and D19S9". Ann Hum Genet. 55 (Pt 3): 225–33. doi:10.1111/j.1469-1809...
Click to read more »cluster with the apolipoprotein C1 (APOC1) gene and the apolipoprotein C2 (APOC2) gene. The APOE gene consists of four exons and three introns, totaling...
Click to read more »HGNC:32152; Q8WW27 868 APOBR HGNC:24087; Q0VD83 869 APOC1 HGNC:607; P02654 870 APOC2 HGNC:609; P02655 871 APOC3 HGNC:610; P02656 872 APOC4 HGNC:611; P55056 873...
Click to read more »that characterise the nature of a blood lipid particle): APOA2, APOC1, APOC2 and APOC3. In 1967 Fredrickson co-authored the paper that described the...
Click to read more »human chromosome 19 linkage group FUT1 (H), FUT2 (SE), LE, LU, PEPD, C3, APOC2, D19S7 and D19S9". Annals of Human Genetics. 55 (Pt 3): 225–33. doi:10.1111/j...
Click to read more »"Apolipoprotein gene cluster on chromosome 19. Definite localization of the APOC2 gene and the polymorphic Hpa I site associated with type III hyperlipoproteinemia"...
Click to read more »gene consisting of 3 exons and 2 introns; it is located 0.5 kb 5' to the APOC2 gene. GRCh38: Ensembl release 89: ENSG00000267467 – Ensembl, May 2017 GRCm38:...
Click to read more »Coghlan G, et al. (1989). "The chromosome 19 linkage group LDLR, C3, LW, APOC2, LU, SE in man". Ann. Hum. Genet. 52 (Pt 2): 137–44. doi:10.1111/j.1469-1809...
Click to read more »capillary malformations; 116860; CCM1 Hyperlipoproteinemia, type Ib; 207750; APOC2 Hyperlysinemia; 238700; AASS Hypermethioninemia, persistent, autosomal dominant...
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