V28M_human-LCAT

General

Gene Locus : human-LCAT

Mode of mutation : Natural mutant

Disease : Lecithin-cholesterol acyltransferase deficiency (LCATD) and fish-eye disease (FED)

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 : c.154G>A Exon 2 Phenotype (LCATD)

References (1)

Title : Stability of lipids on peritoneal dialysis in a patient with familial LCAT deficiency -
Author(s) : Weber CL , Frohlich J , Wang J , Hegele RA , Chan-Yan C
Ref : Nephrol Dial Transplant , 22 :2084 , 2007
PubMedID: 17452402