Gene Locus : human-NLGN2
Mode of mutation : Natural mutant
Disease : Neuroligin 2 Suceptibility Schizophrenia, anxiety, autism, intellectual disability, hyperphagia, and obesity
Summary : Natural mutation\;nonsense variant\;Parente_2017_Am.J.Med.Genet.A_173_213
AAA Change :
Allelic Variant :
Risk Factor :
Inhibitor :
Structure :
Disease by interaction :
Interact Gene Locus :
Xenobiotic sensitivity :
Modification :
Torpedo_number : 100
Kinetic Parameter : No kinetic parameter
News : No news
Comment : c.441C>A p.(Tyr147Ter)
| Title : Neuroligin 2 nonsense variant associated with anxiety, autism, intellectual disability, hyperphagia, and obesity - Parente_2017_Am.J.Med.Genet.A_173_213 |
| Author(s) : Parente DJ , Garriga C , Baskin B , Douglas G , Cho MT , Araujo GC , Shinawi M |
| Ref : American Journal of Medicine Genet A , 173 :213 , 2017 |
| Abstract : Parente_2017_Am.J.Med.Genet.A_173_213 |
| ESTHER : Parente_2017_Am.J.Med.Genet.A_173_213 |
| PubMedSearch : Parente_2017_Am.J.Med.Genet.A_173_213 |
| PubMedID: 27865048 |
| Gene_locus related to this paper: human-NLGN2 |