S21PfsX91_human-CTSA

General

Gene Locus : human-CTSA

Mode of mutation : Natural mutant

Disease : Galactosialidosis

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 :
exon 1 (c60delG) in codon 20, LLVS->LLVP leading to a premature stop codon within 273 bases. Found in a compound heterozygote with IVS2+1G>T

References (1)

Title : New mutations in the PPBG gene lead to loss of PPCA protein which affects the level of the beta-galactosidase\/neuraminidase complex and the EBP-receptor - Malvagia_2004_Mol.Genet.Metab_82_48
Author(s) : Malvagia S , Morrone A , Caciotti A , Bardelli T , d'Azzo A , Ancora G , Zammarchi E , Donati MA
Ref : Mol Genet Metab , 82 :48 , 2004
Abstract :
PubMedSearch : Malvagia_2004_Mol.Genet.Metab_82_48
PubMedID: 15110321
Gene_locus related to this paper: human-CTSA