C99X_human-ABHD5

General

Gene Locus : human-ABHD5

Mode of mutation : Natural mutant

Disease : Chanarin-Dorfman syndrome

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.C99X pCys99Ter c.297C> A homozygous patient with scaly skin lesions since birth, gradually progressing abdominal distention since one and half years of age and delayed motor development

References (1)

Title : Chanarin Dorfman syndrome: a case report with novel nonsense mutation - Gupta_2016_Gene_575_359
Author(s) : Gupta N , Gothwal S , Satpathy AK , Missaglia S , Tavian D , Das P , Timila D , Kabra M
Ref : Gene , 575 :359 , 2016
Abstract : Gupta_2016_Gene_575_359
ESTHER : Gupta_2016_Gene_575_359
PubMedSearch : Gupta_2016_Gene_575_359
PubMedID: 26353074
Gene_locus related to this paper: human-ABHD5