L307P_human-BCHE

General

Gene Locus : human-BCHE

Mode of mutation : Natural mutant

Disease :

Summary : Natural mutation Silent variant Manoharan_2006_Pharmacogenet.Genomics_16_461

AAA Change :

Allelic Variant :

Risk Factor :

Inhibitor :

Structure :

Disease by interaction :

Interact Gene Locus :

Xenobiotic sensitivity : Defect in Suxamethonium hydrolysis

Modification : Silent variant Natural mutation

Torpedo_number : 309

Kinetic Parameter : No kinetic parameter

News : JULY-05-2006

Comment : p.L307P Leu307Pro c920T>C (p.L335P Leu335Pro in primary sequence with 28 amino-acids signal peptide) Silent variant

References (3)

Title : The allele frequency of T920C mutation in butyrylcholinesterase gene is high in an Indian population - David_2015_Gene_555_409
Author(s) : David SM , Soundararajan L , Boopathy R
Ref : Gene , 555 :409 , 2015
Abstract : David_2015_Gene_555_409
ESTHER : David_2015_Gene_555_409
PubMedSearch : David_2015_Gene_555_409
PubMedID: 25447891

Title : A medical health report on individuals with silent butyrylcholinesterase in the Vysya community of India - Manoharan_2007_Clin.Chim.Acta_378_128
Author(s) : Manoharan I , Boopathy R , Darvesh S , Lockridge O
Ref : Clinica Chimica Acta , 378 :128 , 2007
Abstract : Manoharan_2007_Clin.Chim.Acta_378_128
ESTHER : Manoharan_2007_Clin.Chim.Acta_378_128
PubMedSearch : Manoharan_2007_Clin.Chim.Acta_378_128
PubMedID: 17182021

Title : Naturally occurring mutation Leu307Pro of human butyrylcholinesterase in the Vysya community of India - Manoharan_2006_Pharmacogenet.Genomics_16_461
Author(s) : Manoharan I , Wieseler S , Layer PG , Lockridge O , Boopathy R
Ref : Pharmacogenet Genomics , 16 :461 , 2006
Abstract : Manoharan_2006_Pharmacogenet.Genomics_16_461
ESTHER : Manoharan_2006_Pharmacogenet.Genomics_16_461
PubMedSearch : Manoharan_2006_Pharmacogenet.Genomics_16_461
PubMedID: 16788378
Gene_locus related to this paper: human-BCHE