L392PfsX25_human-LPL

General

Gene Locus : human-LPL, human-LPL, human-LPL

Mode of mutation : Natural mutant

Disease : Hyperlipoproteinemia TypeI

Summary :

AAA Change :

Allelic Variant :

Risk Factor :

Inhibitor :

Structure :

Disease by interaction :

Interact Gene Locus :

Xenobiotic sensitivity :

Modification :

Torpedo_number : No torpedo number

Kinetic Parameter : No kinetic parameter

News : No news

Comment :
c.1172_1173insTCCACAAATAAGA (p.Leu392ProfsTer25),homozygous frameshift variant 43-year-old man with longstanding severe hypertriglyceridemia and recurrent acute pancreatitis

References (3)

Title : Clinical and molecular characterization of 2 novel LPL variants in familial chylomicronemia syndrome - Agirbasli_2026_J.Clin.Lipidol__
Author(s) : Agirbasli D , Karaoglan B , Ozalp NH , Kalayci A
Ref : J Clin Lipidol , : , 2026
Abstract :
PubMedSearch : Agirbasli_2026_J.Clin.Lipidol__
PubMedID: 42236341
Gene_locus related to this paper: human-LPL

Title : Clinical and molecular characterization of 2 novel LPL variants in familial chylomicronemia syndrome - Agirbasli_2026_J.Clin.Lipidol__
Author(s) : Agirbasli D , Karaoglan B , Ozalp NH , Kalayci A
Ref : J Clin Lipidol , : , 2026
Abstract :
PubMedSearch : Agirbasli_2026_J.Clin.Lipidol__
PubMedID: 42236341
Gene_locus related to this paper: human-LPL

Title : Clinical and molecular characterization of 2 novel LPL variants in familial chylomicronemia syndrome - Agirbasli_2026_J.Clin.Lipidol__
Author(s) : Agirbasli D , Karaoglan B , Ozalp NH , Kalayci A
Ref : J Clin Lipidol , : , 2026
Abstract :
PubMedSearch : Agirbasli_2026_J.Clin.Lipidol__
PubMedID: 42236341
Gene_locus related to this paper: human-LPL