AutismKB 2.0

Variant Details for NLGN4X


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Basic Information Top
Gene Symbol:NLGN4X ( ASPGX2,AUTSX2,HLNX,HNLX,KIAA1260,MGC22376,NLGN,NLGN4 )
Gene Full Name: neuroligin 4, X-linked
Band: Xp22.32-p22.31
Quick LinksEntrez ID:57502; OMIM: 300427; Uniprot ID:NLGNX_HUMAN; ENSEMBL ID: ENSG00000146938; HGNC ID: 14287
Relate to Another Database: SFARIGene; denovo-db
Variant Statistic Top

Click the link of the category-specific score to view different category of evidences. The categories without any evidences are hidden by default. Chromosome coordinates: hg19
Genetic Category CNVs/SVs de novo Mutations Mosaics SNVs NGS Other Mutations Low-Scale Gene Mutations Linkage Regions Total
Number 6 0 0 0 9 0 15
CNVs/SVs Top
CNV ID Chr Band Start End Size Gain/Loss UCSC Browser Reference
AutCNV0000301 X Xp22 920589 12345395 11424806 loss external link Thomas, 1999
AutCNV0000300 X Xp22 920589 9639551 8718962 loss external link Thomas, 1999
AutCNV0000299 X Xp22 620645 8740227 8119582 loss external link Thomas, 1999
AutCNV0000161 X Xp22.33-22.31 94419 5999994 5905575 loss external link Marshall, 2008
AutCNV0004398 X Xp22.32-p22.33 94419 5849730 5755311 loss external link Sanders, 2011
AutCNV0000713 X Xp11.2-p22.33 60000 56583275 56523275 gain external link Edens, 2011
NGS de novo Mutations Top
iFish (integrated Functional inference of SNVs in human) is based on gene/gene family customized models to classify missense mutations.
Chr Pos Ref Alt Coding AA Validated Method iFish Prediction iFish Probability Reference
No related data!
NGS Mosaic Mutations Top
Chr Position Ref Alt Genotype Validated Method Reference
No related data!
NGS Other Mutations Top
Chr Pos Ref Alt Coding AA Validated iFish Prediction iFish Probability Reference
No related data!
Low-Scale Gene Mutations Top
Chr Pos Ref Alt Coding AA Validated iFish Prediction iFish Probability Reference
X 5821465_5821466 c.1253_1254delAG Bonnet-Brilhault F, 2016
X 6146223 C T Bonnet-Brilhault F, 2016
Laumonnier, 2004
Yan, 2005
Lawson-Yuen, 2008
Daoud, 2009
Pampanos, 2009
Zhang, 2009
c. N Volaki K, 2013
Linkage Regions Top
Linkage Name Band Chr Marker LOD NPL P Value Reference
No related data!




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Syndromic Genes

Non-syndromic Genes

AutismKB Statistics

  • Studies: 1,036
  • Genes: 1,379
  • CNVs/SVs: 5,420
  • SNVs/Indels: 11,669
  • de novo Mutations: 5,669
  • Mosaics: 789
  • Linkage Regions: 172
  • Paper Collected: 6/30/2018
  • Last Update: 8/26/2018