G77fsX5_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.G77fsX82 Gly77fsTer5 (c.230 ins35nt,del c232-245) compound heterozygote with c.894 G>A (S275_Q298del E8SJM) and a novel complex insertion\/deletion leading to a premature termination codon at position 82. G56fsX5 Gly56fsX5 in mature prot c.230-33_230dup\;c232_245del

References (2)

Title : Lysosomal Acid Lipase Deficiency in 23 Spanish Patients: High Frequency of the Novel c.966+2T>G Mutation in Wolman Disease - Ruiz-Andres_2017_JIMD.Rep_37_7
Author(s) : Ruiz-Andres C , Selles E , Arias A , Gort L
Ref : JIMD Rep , 37 :7 , 2017
Abstract :
PubMedSearch : Ruiz-Andres_2017_JIMD.Rep_37_7
PubMedID: 28220406
Gene_locus related to this paper: human-LIPA

Title : Cholesteryl Ester Storage Disease (CESD) due to novel mutations in the LIPA gene - Pisciotta_2009_Mol.Genet.Metab_97_143
Author(s) : Pisciotta L , Fresa R , Bellocchio A , Pino E , Guido V , Cantafora A , Di Rocco M , Calandra S , Bertolini S
Ref : Mol Genet Metab , 97 :143 , 2009
Abstract :
PubMedSearch : Pisciotta_2009_Mol.Genet.Metab_97_143
PubMedID: 19307143
Gene_locus related to this paper: human-LIPA