T441K_human-collq

General

Gene Locus : No gene locus

Mode of mutation : Natural mutant

Disease :

Summary : Natural mutation Congenital myasthenic syndrome associated with endplate AChE deficiency (Type Ic).No attachment to NMJ, No asymetric A12 forms Muller_2004_Neuropediatrics_35_183

AAA Change :

Allelic Variant :

Risk Factor :

Inhibitor :

Structure :

Disease by interaction : Endplate Acetylcholinesterase deficiency\; EAD

Interact Gene Locus : human-collq

Xenobiotic sensitivity :

Modification : Congenital myasthenic syndrome || Natural mutation

Torpedo_number : No torpedo number

Kinetic Parameter : No kinetic parameter

News : JULY-12-2004

Comment : p.Thr441Lys

References (1)

Title : Synaptic congenital myasthenic syndrome in three patients due to a novel missense mutation (T441A) of the COLQ gene - Muller_2004_Neuropediatrics_35_183
Author(s) : Muller JS , Petrova S , Kiefer R , Stucka R , Konig C , Baumeister SK , Huebner A , Lochmuller H , Abicht A
Ref : Neuropediatrics , 35 :183 , 2004
Abstract : Muller_2004_Neuropediatrics_35_183
ESTHER : Muller_2004_Neuropediatrics_35_183
PubMedSearch : Muller_2004_Neuropediatrics_35_183
PubMedID: 15248101