P10Q_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.101C>A

References (1)

Title : Two novel molecular defects in the LCAT gene are associated with fish eye disease - Kuivenhoven_1996_Arterioscler.Thromb.Vasc.Biol_16_294
Author(s) : Kuivenhoven JA , Stalenhoef AF , Hill JS , Demacker PN , Errami A , Kastelein JJ , Pritchard PH
Ref : Arterioscler Thromb Vasc Biol , 16 :294 , 1996
Abstract : Kuivenhoven_1996_Arterioscler.Thromb.Vasc.Biol_16_294
ESTHER : Kuivenhoven_1996_Arterioscler.Thromb.Vasc.Biol_16_294
PubMedSearch : Kuivenhoven_1996_Arterioscler.Thromb.Vasc.Biol_16_294
PubMedID: 8620346