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.1403+4A>G    p.?     splice site     LOF     48      heterozygous    Rumania || p.G339R p.Gly339Arg c.1015G>C mutation located on exon 10 of the SERAC1 two male siblings of consanguineous Turkish parents
| Title : A novel mutation in the SERAC1 gene correlates with the severe manifestation of the MEGDEL phenotype, as revealed by whole-exome sequencing - Alagoz_2020_Exp.Ther.Med_19_3505 | 
| Author(s) : Alagoz M , Kherad N , Turkmen S , Bulut H , Yuksel A | 
| Ref : Exp Ther Med , 19 :3505 , 2020 | 
| Abstract : | 
| PubMedSearch : Alagoz_2020_Exp.Ther.Med_19_3505 | 
| PubMedID: 32346411 | 
| Gene_locus related to this paper: human-SERAC1 |