G365R_human-BCHE

General

Gene Locus : human-BCHE

Mode of mutation : Natural mutant

Disease :

Summary : Silent variant\; Natural mutation,Silent phenotype Non-producer\;Primo-Parmo_1996_Am.J.Hum.Genet_58_52,Maekawa_1995_Clin.Chim.Acta_235_41, Hidaka_1992_Rinsho.Byori_40_535 || Silent variant\; Natural mutation,Silent phenotype\;Maekawa_1995_Clin.Chim.Acta_235_41 || Silent variant\; Natural mutation,Silent phenotype\;Hidaka_1992_Rinsho.Byori_40_535

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 || Natural mutation

Torpedo_number : 367

Kinetic Parameter : No kinetic parameter

News : No news

Comment : p.G365R Gly365Arg (p.G393R Gly393Arg in primary sequence with 28 amino-acids signal peptide) the most frequent mutation in Japanese also found as compound heterozygote with Alu sequence insertion Maekawa_2004. Compound heterozygote for (Gly365Arg) and K-variant (Ala539Thr) in a 52-year-old man undergoing dialysis Tokunaga 2024

References (14)

Title : The First-Known Case of Hereditary Heterozygous Butyrylcholinesterase Deficiency in a Patient on Dialysis - Tokunaga_2024_Cureus_16_e53153
Author(s) : Tokunaga N , Shima H , Okamoto T , Maekawa M , Minakuchi J
Ref : Cureus , 16 :e53153 , 2024
Abstract : Tokunaga_2024_Cureus_16_e53153
ESTHER : Tokunaga_2024_Cureus_16_e53153
PubMedSearch : Tokunaga_2024_Cureus_16_e53153
PubMedID: 38420074

Title : Problem with detection of an insertion-type mutation in the BCHE gene in a patient with butyrylcholinesterase deficiency -
Author(s) : Maekawa M , Taniguchi T , Ishikawa J , Toyoda S , Takahata N
Ref : Clinical Chemistry , 50 :2410 , 2004
PubMedID: 15563496

Title : Gene analysis of genomic DNA from stored serum by polymerase chain reaction: identification of three missense mutations in patients with cholinesterasemia and ABO genotyping - Hidaka_2001_Clin.Chim.Acta_303_61
Author(s) : Hidaka K , Watanabe Y , Tomita M , Ueda N , Higashi M , Minatogawa Y , Iuchi I
Ref : Clinica Chimica Acta , 303 :61 , 2001
Abstract : Hidaka_2001_Clin.Chim.Acta_303_61
ESTHER : Hidaka_2001_Clin.Chim.Acta_303_61
PubMedSearch : Hidaka_2001_Clin.Chim.Acta_303_61
PubMedID: 11163024

Title : Identification of Missense Mutation (G365R) of the Butyrylcholinesterase (BCHE) Gene in a Japanese Patient with Familial Cholinesterasemia - Sakamoto_2001_Kobe.J.Med.Sci_47_153
Author(s) : Sakamoto N , Maeda T , Hidaka K , Teranishi T , Toyoda M , Onishi Y , Kuroda S , Sakaguchi K , Fujisawa T , Maeda M , Watanabe Y , Iuchi I
Ref : Kobe J Med Sci , 47 :153 , 2001
Abstract : Sakamoto_2001_Kobe.J.Med.Sci_47_153
ESTHER : Sakamoto_2001_Kobe.J.Med.Sci_47_153
PubMedSearch : Sakamoto_2001_Kobe.J.Med.Sci_47_153
PubMedID: 11733654

Title : Three point mutations of human butyrylcholinesterase in a Japanese family and the alterations of three-dimensional structure - Asanuma_1999_Clin.Chim.Acta_283_33
Author(s) : Asanuma K , Yagihashi A , Uehara N , Kida T , Watanabe N
Ref : Clinica Chimica Acta , 283 :33 , 1999
Abstract : Asanuma_1999_Clin.Chim.Acta_283_33
ESTHER : Asanuma_1999_Clin.Chim.Acta_283_33
PubMedSearch : Asanuma_1999_Clin.Chim.Acta_283_33
PubMedID: 10404729

Title : Butyrylcholinesterase genes in individuals with abnormal inhibition numbers and with trace activity: one common mutation and two novel silent genes - Dey_1998_Ann.Clin.Biochem_35_302
Author(s) : Dey DC , Maekawa M , Sudo K , Kanno T
Ref : Annals of Clinical Biochemistry , 35 :302 , 1998
Abstract : Dey_1998_Ann.Clin.Biochem_35_302
ESTHER : Dey_1998_Ann.Clin.Biochem_35_302
PubMedSearch : Dey_1998_Ann.Clin.Biochem_35_302
PubMedID: 9547905
Gene_locus related to this paper: human-BCHE

Title : Genetic mutations of butyrylcholine esterase identified from phenotypic abnormalities in Japan - Maekawa_1997_Clin.Chem_43_924
Author(s) : Maekawa M , Sudo K , Dey DC , Ishikawa J , Izumi M , Kotani K , Kanno T
Ref : Clinical Chemistry , 43 :924 , 1997
Abstract : Maekawa_1997_Clin.Chem_43_924
ESTHER : Maekawa_1997_Clin.Chem_43_924
PubMedSearch : Maekawa_1997_Clin.Chem_43_924
PubMedID: 9191541

Title : Characterization of 12 silent alleles of the human butyrylcholinesterase (BCHE) gene - Primo-Parmo_1996_Am.J.Hum.Genet_58_52
Author(s) : Primo-Parmo SL , Bartels CF , Wiersema B , van der Spek AF , Innis JW , La Du BN
Ref : American Journal of Human Genetics , 58 :52 , 1996
Abstract : Primo-Parmo_1996_Am.J.Hum.Genet_58_52
ESTHER : Primo-Parmo_1996_Am.J.Hum.Genet_58_52
PubMedSearch : Primo-Parmo_1996_Am.J.Hum.Genet_58_52
PubMedID: 8554068

Title : Three different point mutations in the butyrylcholinesterase gene of three Japanese subjects with a silent phenotype: possible Japanese type alleles - Sudo_1996_Clin.Biochem_29_165
Author(s) : Sudo K , Maekawa M , Kanno T , Akizuki S , Magara T
Ref : Clinical Biochemistry , 29 :165 , 1996
Abstract : Sudo_1996_Clin.Biochem_29_165
ESTHER : Sudo_1996_Clin.Biochem_29_165
PubMedSearch : Sudo_1996_Clin.Biochem_29_165
PubMedID: 8601326

Title : Genetic basis of the silent phenotype of serum butyrylcholinesterase in three compound heterozygotes - Maekawa_1995_Clin.Chim.Acta_235_41
Author(s) : Maekawa M , Sudo K , Kanno T , Kotani K , Dey DC , Ishikawa J , Izumi M , Etoh K
Ref : Clinica Chimica Acta , 235 :41 , 1995
Abstract : Maekawa_1995_Clin.Chim.Acta_235_41
ESTHER : Maekawa_1995_Clin.Chim.Acta_235_41
PubMedSearch : Maekawa_1995_Clin.Chim.Acta_235_41
PubMedID: 7634491

Title : [Gene analysis of human cholinesterase variants]. - Muratani_1993_Japanese.J.Clin.Med_51_495
Author(s) : Muratani K , Hada T , Higashino K
Ref : Nippon Rinsho Japanese Journal of Clinical Medicine , 51 :495 , 1993
Abstract : Muratani_1993_Japanese.J.Clin.Med_51_495
ESTHER : Muratani_1993_Japanese.J.Clin.Med_51_495
PubMedSearch : Muratani_1993_Japanese.J.Clin.Med_51_495
PubMedID: 8464162

Title : Heterogeneity of the Silent Phenotype of Human Butyrylcholinesterase - Identification of Eight New Mutations -
Author(s) : Primo-Parmo SL , Bartels CF
Ref : In Multidisciplinary approaches to cholinesterase functions - Proceedings of Fourth International Meeting on Cholinesterases , (Shafferman, A. and Velan, B., Eds) Plenum Press, New York :61 , 1992
PubMedID:

Title : [Identification of two different genetic mutation associated with silent phenotypes for human serum cholinesterase in Japanese] - Hidaka_1992_Rinsho.Byori_40_535
Author(s) : Hidaka K , Iuchi I , Yamasaki T , Ohhara M , Shoda T , Primo-Parmo SL , La Du BN
Ref : Rinsho Byori , 40 :535 , 1992
Abstract : Hidaka_1992_Rinsho.Byori_40_535
ESTHER : Hidaka_1992_Rinsho.Byori_40_535
PubMedSearch : Hidaka_1992_Rinsho.Byori_40_535
PubMedID: 1507480

Title : A variant serum cholinesterase and a confirmed point mutation at Gly-365 to Arg found in a patient with liver cirrhosis - Hada_1992_Intern.Med_31_357
Author(s) : Hada T , Muratani K , Ohue T , Imanishi H , Moriwaki Y , Itoh M , Amuro Y , Higashino K
Ref : Intern Med , 31 :357 , 1992
Abstract : Hada_1992_Intern.Med_31_357
ESTHER : Hada_1992_Intern.Med_31_357
PubMedSearch : Hada_1992_Intern.Med_31_357
PubMedID: 1611188