G42E_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.(Gly42Glu) c.125G>A Exon2. rs386833631 CM981625

References (2)

Title : Biochemical analysis of mutations in palmitoyl-protein thioesterase causing infantile and late-onset forms of neuronal ceroid lipofuscinosis - Das_2001_Hum.Mol.Genet_10_1431
Author(s) : Das AK , Lu JY , Hofmann SL
Ref : Hum Mol Genet , 10 :1431 , 2001
Abstract : Das_2001_Hum.Mol.Genet_10_1431
ESTHER : Das_2001_Hum.Mol.Genet_10_1431
PubMedSearch : Das_2001_Hum.Mol.Genet_10_1431
PubMedID: 11440996
Gene_locus related to this paper: human-PPT1

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 : Das_1998_J.Clin.Invest_102_361
ESTHER : Das_1998_J.Clin.Invest_102_361
PubMedSearch : Das_1998_J.Clin.Invest_102_361
PubMedID: 9664077
Gene_locus related to this paper: human-PPT1