S286R_human-LPL

General

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.Ser286Arg S286R c.858T>A (Ser259Arg S259R in the mature protein as mentionned in some publications which do not count signal peptide)

References (3)

Title : Familial hypertriglyceridemia: biochemical, clinical and molecular study in a Moroccan family - Bouabdellah_2015_Ann.Biol.Clin.(Paris)_73_474
Author(s) : Bouabdellah M , Iraqi H , Benlian P , Berqia I , Benchekroun L , Chraibi A , Chabraoui L
Ref : Ann Biol Clin (Paris) , 73 :474 , 2015
Abstract : Bouabdellah_2015_Ann.Biol.Clin.(Paris)_73_474
ESTHER : Bouabdellah_2015_Ann.Biol.Clin.(Paris)_73_474
PubMedSearch : Bouabdellah_2015_Ann.Biol.Clin.(Paris)_73_474
PubMedID: 26104879

Title : Spectrum of mutations of the LPL gene identified in Italy in patients with severe hypertriglyceridemia - Rabacchi_2015_Atherosclerosis_241_79
Author(s) : Rabacchi C , Pisciotta L , Cefalu AB , Noto D , Fresa R , Tarugi P , Averna M , Bertolini S , Calandra S
Ref : Atherosclerosis , 241 :79 , 2015
Abstract : Rabacchi_2015_Atherosclerosis_241_79
ESTHER : Rabacchi_2015_Atherosclerosis_241_79
PubMedSearch : Rabacchi_2015_Atherosclerosis_241_79
PubMedID: 25966443
Gene_locus related to this paper: human-LPL

Title : A single Ser259Arg mutation in the gene for lipoprotein lipase causes chylomicronemia in Moroccans of Berber ancestry - Foubert_1997_Hum.Mutat_10_179
Author(s) : Foubert L , Bruin T , De Gennes JL , Ehrenborg E , Furioli J , Kastelein J , Benlian P , Hayden M
Ref : Hum Mutat , 10 :179 , 1997
Abstract : Foubert_1997_Hum.Mutat_10_179
ESTHER : Foubert_1997_Hum.Mutat_10_179
PubMedSearch : Foubert_1997_Hum.Mutat_10_179
PubMedID: 9298816
Gene_locus related to this paper: human-LPL