M1I_human-PPT1

General

Gene Locus : human-PPT1

Mode of mutation : Natural mutant

Disease : Infantile neuronal ceroid lipofuscinosis

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.(Met1) c.3G>A No Initiation No M1 Exon1 CM981622

References (1)

Title : Molecular genetics of palmitoyl-protein thioesterase deficiency in the U.S - Das_1998_J.Clin.Invest_102_361
Author(s) : Das AK , Becerra CH , Yi W , Lu JY , Siakotos AN , Wisniewski KE , Hofmann SL
Ref : Journal of Clinical Investigation , 102 :361 , 1998
Abstract :
PubMedSearch : Das_1998_J.Clin.Invest_102_361
PubMedID: 9664077
Gene_locus related to this paper: human-PPT1