AutismKB 2.0

Variant Details for VCX2


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Basic Information Top
Gene Symbol:VCX2 ( MGC118977,MGC125729,MGC125794,MGC125795,VCX-2r,VCX2R,VCXB )
Gene Full Name: variable charge, X-linked 2
Band: Xp22.31
Quick LinksEntrez ID:51480; OMIM: 300532; Uniprot ID:VCX2_HUMAN; ENSEMBL ID: ENSG00000177504; HGNC ID: 18158
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 0 0 6
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
AutCNV0000671 X Xp22.1-p22.3 6644160 24159444 17515284 loss external link Vazna, 2010
AutCNV0000713 X Xp11.2-p22.33 60000 56583275 56523275 gain external link Edens, 2011
AutCNV0004967 3 3p14 60472496 67385119 6912623 loss external link Okumura A, 2014
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
No related data!
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