Gene Locus : human-LIPA
Mode of mutation : Natural mutant
Disease : Wolman disease WD, Cholesterol Ester Storage Disease, CESD
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 : Mutation in exon 4: c.294C>G (p.Asn98Lys)
Title : Characterization of the mechanisms by which missense mutations in the lysosomal acid lipase gene disrupt enzymatic activity - Vinje_2019_Hum.Mol.Genet_28_3043 |
Author(s) : Vinje T , Laerdahl JK , Bjune K , Leren TP , Strom TB |
Ref : Hum Mol Genet , 28 :3043 , 2019 |
Abstract : Vinje_2019_Hum.Mol.Genet_28_3043 |
ESTHER : Vinje_2019_Hum.Mol.Genet_28_3043 |
PubMedSearch : Vinje_2019_Hum.Mol.Genet_28_3043 |
PubMedID: 31131398 |
Gene_locus related to this paper: human-LIPA |
Title : Prevalence of cholesteryl ester storage disease among hypercholesterolemic subjects and functional characterization of mutations in the lysosomal acid lipase gene - Vinje_2018_Mol.Genet.Metab_123_169 |
Author(s) : Vinje T , Wierod L , Leren TP , Strom TB |
Ref : Mol Genet Metab , 123 :169 , 2018 |
Abstract : Vinje_2018_Mol.Genet.Metab_123_169 |
ESTHER : Vinje_2018_Mol.Genet.Metab_123_169 |
PubMedSearch : Vinje_2018_Mol.Genet.Metab_123_169 |
PubMedID: 29196158 |
Gene_locus related to this paper: human-LIPA |
Title : Novel LIPA mutations in Mexican siblings with lysosomal acid lipase deficiency - Santillan-Hernandez_2015_World.J.Gastroenterol_21_1001 |
Author(s) : Santillan-Hernandez Y , Almanza-Miranda E , Xin WW , Goss K , Vera-Loaiza A , Gorraez-de la Mora MT , Pina-Aguilar RE |
Ref : World J Gastroenterol , 21 :1001 , 2015 |
Abstract : Santillan-Hernandez_2015_World.J.Gastroenterol_21_1001 |
ESTHER : Santillan-Hernandez_2015_World.J.Gastroenterol_21_1001 |
PubMedSearch : Santillan-Hernandez_2015_World.J.Gastroenterol_21_1001 |
PubMedID: 25624737 |
Gene_locus related to this paper: human-LIPA |