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
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 |