- Analytes
- PCSK9
PCSK9
Name: |
proprotein convertase subtilisin/kexin type 9
|
Symbol: |
PCSK9
|
Version of Orphanet: |
2023-06-22 14:14:43
|
Synonyms: |
FH3
NARC-1
|
XREF(s): | |
Created: |
13 May 2019 - 01:01
|
Changed: |
22 Jun 2023 - 16:14
|
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Dyslipidemia ( 13 genes) - ULB
Gene % of coding sequence sufficiently covered to detect heterozygous mutations Copy number variation Comments ABCG5 100.00 1 In case of hypercholesterolemia / NM_022436.2 ABCG8 100.00 1 In case of hypercholesterolemia / NM_022437.2 APOB 100.00 1 In case of hypercholesterolemia / NM_000384.2 APOE 100.00 1 In case of hypercholesterolemia / NM_000041.3 LDLR 100.00 1 In case of hypercholesterolemia / NM_000527.4 LDLRAP1 100.00 1 In case of hypercholesterolemia / NM_015627.2 LIPA 100.00 1 In case of hypercholesterolemia / NM_000235.3 PCSK9 100.00 1 In case of hypercholesterolemia / NM_174936.3 LPL 100.00 1 In case of hypertriglyceridemia / NM_000237.2 APOC2 100.00 1 In case of hypertriglyceridemia / NM_000483.4 APOA5 100.00 1 In case of hypertriglyceridemia / NM_052968.4 GPIHBP1 100.00 1 In case of hypertriglyceridemia / NM_178172.5 LMF1 100.00 1 In case of hypertriglyceridemia / NM_022773.3 -
Familial Hypercholesterolemia (9 genes) - IPG
Gene % of coding sequence sufficiently covered to detect heterozygous mutations Copy number variation Comments APOB 100.00 1 NM_000384.3 APOE 100.00 1 NM_000041.4 LDLR 100.00 1 NM_000527.5 LDLRAP1 100.00 1 NM_015627.3 PCSK9 100.00 1 NM_174936.4 ABCG5 100.00 1 NM_022436.3 ABCG8 100.00 1 NM_022437.3 LIPA 100.00 1 NM_000235.4 STAP1 100.00 1 NM_012108.4 -
Familial Hypercholesterolemia panel (4 genes) - KUL
Gene % of coding sequence sufficiently covered to detect heterozygous mutations Copy number variation Comments LDLR 100.00 1 APOB 100.00 1 APOE 100.00 1 PCSK9 100.00 1 -
Familial Hypercholesterolemia panel (8 genes) - UZA
Gene % of coding sequence sufficiently covered to detect heterozygous mutations Copy number variation Comments LDLR APOB APOE PCSK9 LDLRAP1 LIPA ABCG5 ABCG8 -
Familial Hypercholesterolemia panel (9 genes) - ULG
Gene % of coding sequence sufficiently covered to detect heterozygous mutations Copy number variation Comments LDLR 100.00 1 only for 5'UTR + coding exons + intronic borders +/-14pb APOB 99.79 0 only for coding exons and intronic borders +/-14pb Exons 26 and 29 are entirely covered at 30x Exon 1 is not covered APOE 100.00 0 only for coding exons and intronic borders +/-14pb PCSK9 100.00 0 only for coding exons and intronic borders +/-14pb LDLRAP1 98.69 0 only for coding exons and intronic borders +/-14pb exon 1 is not covered LIPA 100.00 0 only for coding exons and intronic borders +/-14pb ABCG5 100.00 0 only for coding exons and intronic borders +/-14pb ABCG8 100.00 0 only for coding exons and intronic borders +/-14pb STAP1 100.00 0 only for coding exons and intronic borders +/-14pb -
Hypercholesterolemia (4 genes) - UZA
Gene % of coding sequence sufficiently covered to detect heterozygous mutations Copy number variation Comments LDLR APOB APOE PCSK9 -
Hypercholesterolemia (9 genes) - UCL
Gene % of coding sequence sufficiently covered to detect heterozygous mutations Copy number variation Comments LDLR 100.00 1 APOB 100.00 1 PCSK9 100.00 1 ABCG5 100.00 1 ABCG8 100.00 1 APOE 100.00 1 LDLRAP1 100.00 1 LIPA 100.00 1 STAP1 100.00 1 -
Hypercholesterolemia, Familial (4 genes) - KUL
Gene % of coding sequence sufficiently covered to detect heterozygous mutations Copy number variation Comments LDLR APOB PCSK9 APOE