W38CfsX12_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.(Trp38CysfsTer12) c.114delG Exon 1 Frameshift

References (2)

Title : Computational and structural investigation of Palmitoyl-Protein Thioesterase 1 (PPT1) protein causing Neuronal Ceroid Lipofuscinoses (NCL) - Thirumal Kumar_2022_Adv.Protein.Chem.Struct.Biol_132_89
Author(s) : Thirumal Kumar D , Shaikh N , Udhaya Kumar S , George Priya Doss C
Ref : Advances in Protein Chemistry Struct Biol , 132 :89 , 2022
Abstract : Thirumal Kumar_2022_Adv.Protein.Chem.Struct.Biol_132_89
ESTHER : Thirumal Kumar_2022_Adv.Protein.Chem.Struct.Biol_132_89
PubMedSearch : Thirumal Kumar_2022_Adv.Protein.Chem.Struct.Biol_132_89
PubMedID: 36088080
Gene_locus related to this paper: human-PPT1

Title : Update of the mutation spectrum and clinical correlations of over 360 mutations in eight genes that underlie the neuronal ceroid lipofuscinoses - Kousi_2012_Hum.Mutat_33_42
Author(s) : Kousi M , Lehesjoki AE , Mole SE
Ref : Hum Mutat , 33 :42 , 2012
Abstract : Kousi_2012_Hum.Mutat_33_42
ESTHER : Kousi_2012_Hum.Mutat_33_42
PubMedSearch : Kousi_2012_Hum.Mutat_33_42
PubMedID: 21990111
Gene_locus related to this paper: human-PPT1