S498T_human-SERAC1

General

Gene Locus : human-SERAC1

Mode of mutation : Natural mutant

Disease : MEGDEL 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 :
c.1493G>C p.Ser498Thr Missense

References (2)

Title : MEGDEL Syndrome and Its Anesthetic Implications - Horvath_2021_Cureus_13_e17761
Author(s) : Horvath B , Pfister KM , Rupp A , Kloesel B
Ref : Cureus , 13 :e17761 , 2021
Abstract :
PubMedSearch : Horvath_2021_Cureus_13_e17761
PubMedID: 34540505
Gene_locus related to this paper: human-SERAC1

Title : Mutations in the phospholipid remodeling gene SERAC1 impair mitochondrial function and intracellular cholesterol trafficking and cause dystonia and deafness - Wortmann_2012_Nat.Genet_44_797
Author(s) : Wortmann SB , Vaz FM , Gardeitchik T , Vissers LE , Renkema GH , Schuurs-Hoeijmakers JH , Kulik W , Lammens M , Christin C , Kluijtmans LA , Rodenburg RJ , Nijtmans LG , Grunewald A , Klein C , Gerhold JM , Kozicz T , van Hasselt PM , Harakalova M , Kloosterman W , Baric I , Pronicka E , Ucar SK , Naess K , Singhal KK , Krumina Z , Gilissen C , van Bokhoven H , Veltman JA , Smeitink JA , Lefeber DJ , Spelbrink JN , Wevers RA , Morava E , de Brouwer AP
Ref : Nat Genet , 44 :797 , 2012
Abstract :
PubMedSearch : Wortmann_2012_Nat.Genet_44_797
PubMedID: 22683713
Gene_locus related to this paper: human-SERAC1