G14X_human-ABHD5

General

Gene Locus : human-ABHD5

Mode of mutation :

Disease : NAFLD || Chanarin-Dorfman syndrome

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.Gly14Ter c.40G>T in exon 1. Heterozygous nonsense mutation in 9 affected patients with Non-alcoholic fatty liver disease (NAFLD) in a large non-consanguineous family of Italian ancestry

References (1)

Title : Inherited non-alcoholic fatty liver disease and dyslipidemia due to monoallelic ABHD5 mutations - Youssefian_2019_J.Hepatol_71_366
Author(s) : Youssefian L , Vahidnezhad H , Saeidian AH , Pajouhanfar S , Sotoudeh S , Mansouri P , Amirkashani D , Zeinali S , Levine MA , Peris K , Colombo R , Uitto J
Ref : Journal of Hepatology , 71 :366 , 2019
Abstract : Youssefian_2019_J.Hepatol_71_366
ESTHER : Youssefian_2019_J.Hepatol_71_366
PubMedSearch : Youssefian_2019_J.Hepatol_71_366
PubMedID: 30954460
Gene_locus related to this paper: human-ABHD5