Full data view for gene PLG

Information The variants shown are described using the NM_000301.3 transcript reference sequence.

4 entries on 1 page. Showing entries 1 - 4.
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+/+ 9 c.988A>G r.(?) p.(Lys330Glu) Maternal (confirmed) ACMG pathogenic g.161139762A>G g.160718730A>G - - PLG_000046 - Journal: Bork 2020 ClinVar-RCV001507288.6 rs889957249 Germline - 0.00004 (gnomAD_exome), 0.00003 (gnomAD) - - - DNA SEQ blood - HAE4 - Journal: Bork 2020 One family with compound heterozygous individuals and 12 affected patients - - Germany - - - - - 12 Christian Drouet
+/+ 9 c.988A>G r.(?) p.(Lys330Glu) Unknown ACMG pathogenic g.161139762A>G g.160718730A>G - - PLG_000046 ACMG classification: Characterized as Class 5 (pathogenic) by ghardy Bork 2018: 13 families with 60 affected individuals Bork 2023: Occurrence of only one symptomatic patient per family, who had no family history of angioedema but who had symptom-free relatives carrying the same HAE-linked c.988A>G variant. Hintze 2023 concluded that the kallikrein-kinin system is bypassed in HAE-PLG. Structural modeling and in vitro assays confirmed the PLG mutation c.988A>G; p.Lys330Glu to be a gain of function mutation resulting in an increased bradykinin release by direct HK cleavage. Bork 2025: Hypertension risk for carriers of c.988A>G variant. Journal: Bork 2018 Journal: Bork 2020 Journal: Bork 2023 Journal: Hintze 2023 Journal: Bork 2025 ClinVar-RCV001507288.6 rs889957249 Germline/De novo (untested) yes 0.00004 (gnomAD_exome), 0.00003 (gnomAD), 6.98e-06 (gnomAD v3) - - - DNA SEQ blood - HAE4 - Journal: Bork 2018 Journal: Bork 2023 Journal: Hintze 2023 Bork 2018: Thirteen families with 60 affected individuals Bork 2023: Six German pedigrees have been found to carry a c.988A>G; solitary German carriers (n=6) Hintze 2023: a German pedigree with 8 affected individuals - no Germany - - - - - 74 Christian Drouet
+/+ 9 c.988A>G r.(?) p.(Lys330Glu) Both (homozygous) ACMG pathogenic g.161139762A>G g.160718730A>G - - PLG_000046 Homozygous or heterozygous (n = 8) carriers of p.(Lys330Glu) display a significantly high susceptibility to the PLG activation by streptokinase and urokinase Journal: Germenis 2018 Journal: Parsopoulou 2020 ClinVar-RCV001507288.6 rs889957249 Germline yes 0.000004 (gnomAD_exome); 0.00003 (gnomAD) - - - DNA SEQ-NG-IT - - HAE4 - Journal: Germenis 2018 A single pedigree has been found as carrying a c.988A>G variant; the female proband is a homozygous carrier, 2 heterozygous carriers have been found asymptomatic. F ? Greece - - - - - 3 Christian Drouet
+/+ 9 c.988A>G r.(?) p.(Lys330Glu) Unknown ACMG pathogenic g.161139762A>G g.160718730A>G - - PLG_000046 The heterozygous carriers of the family present with two bands of PLG type I and PLG type II approximately equal intensity and a susceptibility to zymogen activation. The Lys to Glu substitution introduces a Lys-binding site into the PLG kringle 3 domain, propably altering binding to kininogens. Plg residue 311 is Glu in most mammals. Glu311 in patients with HAE represents reversion to the ancestral condition. Substantial BK generation occurs during Plg-Glu311 cleavage of human HK, but not mouse HK. Mouse Plg, which has Glu311, did not liberate BK from human kininogens more rapidly than human PLG-Lys311. This indicates Glu311 is pathogenic in the context of human PLG when human kininogens are the substrates. Journal: Parsopoulou 2020 Journal: Dickeson 2022 ClinVar-RCV001507288.6 rs889957249 Germline yes 0.00003 (gnomAD); 0.000004 (gnomAD_exome) - - - DNA SEQ-NG-IT blood - HAE4 - Journal: Parsopoulou 2020 A Spanish family with 5 heterozygous carriers of a c.988A>G variant, incl 3/5 symptomatic individuals - no Spain - - - - - 3 Christian Drouet
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