N147fs_human-LPL

General

Gene Locus : human-LPL

Mode of mutation : Natural mutant

Disease : Hyperlipoproteinemia TypeI

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.N147fs Asn147fs del 614ACTA617 (N120fs Asn120fs frameshift stop142 in the mature protein which do not count signal peptide)

References (2)

Title : Compound heterozygosity for frameshift mutations in the gene for lipoprotein lipase in a patient with early-onset chylomicronemia -
Author(s) : Foubert L , De Gennes JL , Benlian P , Truffert J , Miao L , Hayden MR
Ref : Hum Mutat , Suppl 1 :S141 , 1998
PubMedID: 9452069

Title : Assessment of French patients with LPL deficiency for French Canadian mutations - Foubert_1997_J.Med.Genet_34_672
Author(s) : Foubert L , De Gennes JL , Lagarde JP , Ehrenborg E , Raisonnier A , Girardet JP , Hayden MR , Benlian P
Ref : Journal of Medical Genetics , 34 :672 , 1997
Abstract : Foubert_1997_J.Med.Genet_34_672
ESTHER : Foubert_1997_J.Med.Genet_34_672
PubMedSearch : Foubert_1997_J.Med.Genet_34_672
PubMedID: 9279761