IVS6-1G>T_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.Exon skipping c.628-1G>T Intron6. Aberrant splicing Splice site CS000593

References (2)

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

Title : Detection of eight novel palmitoyl protein thioesterase (PPT) mutations underlying infantile neuronal ceroid lipofuscinosis (INCL\;CLN1) - Salonen_2000_Hum.Mutat_15_273
Author(s) : Salonen T , Jarvela I , Peltonen L , Jalanko A
Ref : Hum Mutat , 15 :273 , 2000
Abstract : Salonen_2000_Hum.Mutat_15_273
ESTHER : Salonen_2000_Hum.Mutat_15_273
PubMedSearch : Salonen_2000_Hum.Mutat_15_273
PubMedID: 10679943
Gene_locus related to this paper: human-PPT1