C96Y_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.(Cys96Tyr)c.287G>A Exon3 CM011802

References (3)

Title : Atypical juvenile neuronal ceroid lipofuscinosis: A report of three cases - Setty_2013_J.Pediatr.Neurosci_8_117
Author(s) : Setty G , Saleem R , Khan A , Hussain N
Ref : J Pediatr Neurosci , 8 :117 , 2013
Abstract : Setty_2013_J.Pediatr.Neurosci_8_117
ESTHER : Setty_2013_J.Pediatr.Neurosci_8_117
PubMedSearch : Setty_2013_J.Pediatr.Neurosci_8_117
PubMedID: 24082928
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

Title : New mutations in the neuronal ceroid lipofuscinosis genes - Mole_2001_Eur.J.Paediatr.Neurol_5 Suppl A_7
Author(s) : Mole SE , Zhong NA , Sarpong A , Logan WP , Hofmann S , Yi W , Franken PF , van Diggelen OP , Breuning MH , Moroziewicz D , Ju W , Salonen T , Holmberg V , Jarvela I , Taschner PE
Ref : Eur J Paediatr Neurol , 5 Suppl A :7 , 2001
Abstract : Mole_2001_Eur.J.Paediatr.Neurol_5 Suppl A_7
ESTHER : Mole_2001_Eur.J.Paediatr.Neurol_5 Suppl A_7
PubMedSearch : Mole_2001_Eur.J.Paediatr.Neurol_5 Suppl A_7
PubMedID: 11589012
Gene_locus related to this paper: human-PPT1