Gene Locus : 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 : p.Q262X Gln262X c.784C>T (p.Q235X Gln235X in the mature protein) found in a compound heterozygote with R270H
Title : Association of Rare and Common Variation in the Lipoprotein Lipase Gene With Coronary Artery Disease - Khera_2017_JAMA_317_937 |
Author(s) : Khera AV , Won HH , Peloso GM , O'Dushlaine C , Liu D , Stitziel NO , Natarajan P , Nomura A , Emdin CA , Gupta N , Borecki IB , Asselta R , Duga S , Merlini PA , Correa A , Kessler T , Wilson JG , Bown MJ , Hall AS , Braund PS , Carey DJ , Murray MF , Kirchner HL , Leader JB , Lavage DR , Manus JN , Hartzel DN , Samani NJ , Schunkert H , Marrugat J , Elosua R , McPherson R , Farrall M , Watkins H , Lander ES , Rader DJ , Danesh J , Ardissino D , Gabriel S , Willer C , Abecasis GR , Saleheen D , Dewey FE , Kathiresan S |
Ref : Jama , 317 :937 , 2017 |
Abstract : Khera_2017_JAMA_317_937 |
ESTHER : Khera_2017_JAMA_317_937 |
PubMedSearch : Khera_2017_JAMA_317_937 |
PubMedID: 28267856 |
Gene_locus related to this paper: human-LPL |
Title : Incidental finding of severe hypertriglyceridemia in children. Role of multiple rare variants in genes affecting plasma triglyceride - Buonuomo_2017_J.Clin.Lipidol_11_1329 |
Author(s) : Buonuomo PS , Rabacchi C , Macchiaiolo M , Trenti C , Fasano T , Tarugi P , Bartuli A , Bertolini S , Calandra S |
Ref : J Clin Lipidol , 11 :1329 , 2017 |
Abstract : Buonuomo_2017_J.Clin.Lipidol_11_1329 |
ESTHER : Buonuomo_2017_J.Clin.Lipidol_11_1329 |
PubMedSearch : Buonuomo_2017_J.Clin.Lipidol_11_1329 |
PubMedID: 28951076 |
Gene_locus related to this paper: human-LIPC , human-LPL |