I158K_human-NLGN1

General

Gene Locus : No gene locus

Mode of mutation : Natural

Disease :

Summary : Gerik-Celebi_2024_Dev.Neurobiol__

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 :
NLGN1 c.473T>A (p.Ile158Lys)

References (1)

Title : Rare heterozygous genetic variants of NRXN and NLGN gene families involved in synaptic function and their association with neurodevelopmental disorders - Gerik-Celebi_2024_Dev.Neurobiol__
Author(s) : Gerik-Celebi HB , Bolat H , Unsel-Bolat G
Ref : Dev Neurobiol , : , 2024
Abstract :
PubMedSearch : Gerik-Celebi_2024_Dev.Neurobiol__
PubMedID: 38739110