R312X_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 : NOVEMBER-15-2006

Comment : p.R312X p.Arg312Ter c.C934T ichthyosis, liver cirrhosis, and a hearing impairment. Compound heterozygote with c.616_647delinsGGG

References (2)

Title : From blood smear to lipid disorder: a case report - Elitzur_2013_J.Pediatr.Hematol.Oncol_35_e329
Author(s) : Elitzur S , Yacobovich J , Dgany O , Krasnov T , Rosenbach Y , Tamary H
Ref : J Pediatr Hematol Oncol , 35 :e329 , 2013
Abstract : Elitzur_2013_J.Pediatr.Hematol.Oncol_35_e329
ESTHER : Elitzur_2013_J.Pediatr.Hematol.Oncol_35_e329
PubMedSearch : Elitzur_2013_J.Pediatr.Hematol.Oncol_35_e329
PubMedID: 23042024

Title : Erythrokeratoderma variabilis-like ichthyosis in Chanarin-Dorfman syndrome - Pujol_2005_Br.J.Dermatol_153_838
Author(s) : Pujol RM , Gilaberte M , Toll A , Florensa L , Lloreta J , Gonzalez-Ensenat MA , Fischer J , Azon A
Ref : Br J Dermatol , 153 :838 , 2005
Abstract : Pujol_2005_Br.J.Dermatol_153_838
ESTHER : Pujol_2005_Br.J.Dermatol_153_838
PubMedSearch : Pujol_2005_Br.J.Dermatol_153_838
PubMedID: 16181472
Gene_locus related to this paper: human-ABHD5