S127X_human-LIPA

General

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 :
p.S127X Ser127Ter Two homozygotes for a 1-bp deletion introducing a premature in-frame termination codon at amino acid position 127. S106X Ser106Ter in the mature protein

References (1)

Title : Characterization of lysosomal acid lipase mutations in the signal peptide and mature polypeptide region causing Wolman disease - Zschenker_2001_J.Lipid.Res_42_1033
Author(s) : Zschenker O , Jung N , Rethmeier J , Trautwein S , Hertel S , Zeigler M , Ameis D
Ref : J Lipid Res , 42 :1033 , 2001
Abstract :
PubMedSearch : Zschenker_2001_J.Lipid.Res_42_1033
PubMedID: 11441129
Gene_locus related to this paper: human-LIPA