AutismKB 2.0

Variant Details for LINGO2


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Basic Information Top
Gene Symbol:LINGO2 ( FLJ31810,LERN3,LRRN6C )
Gene Full Name: leucine rich repeat and Ig domain containing 2
Band: 9p21.2-p21.1
Quick LinksEntrez ID:158038; OMIM: 609793; Uniprot ID:LIGO2_HUMAN; ENSEMBL ID: ENSG00000174482; HGNC ID: 21207
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 17 1 0 0 0 1 19
CNVs/SVs Top
CNV ID Chr Band Start End Size Gain/Loss UCSC Browser Reference
AutCNV0000088 9 9p21.1 28124200 31359900 3235700 gain external link Szatmari, 2007
AutCNV0000084 9 9p13.3-24.3 249391 33926500 33677109 gain external link Szatmari, 2007
AutCNV0002732 9 9p21.1 28591877 28761593 169716 loss external link Pinto, 2010
AutCNV0001941 9 9p21.1 28677376 28775609 98233 loss external link Pinto, 2010
AutCNV0001940 9 9p21.1 28591877 28761593 169716 loss external link Pinto, 2010
AutCNV0001939 9 9p21.1 28591877 28761593 169716 loss external link Pinto, 2010
AutCNV0001276 9 9p21.1 28591877 28761593 169716 loss external link Pinto, 2010
AutCNV0000960 9 9p21.1 28550756 28582398 31642 loss external link Pinto, 2010
AutCNV0000948 9 9p21.1 28534489 28566849 32360 loss external link Pinto, 2010
AutCNV0003303 9 9p21.1 28519666 28793773 274107 loss external link Gai, 2011
AutCNV0003642 9 9p21.1 28577961 28628500 50539 loss external link Gai, 2011
AutCNV0003641 9 9p21.1 28577961 28620312 42351 loss external link Gai, 2011
AutCNV0003306 9 9p21.1 28550930 28585455 34525 loss external link Gai, 2011
AutCNV0003305 9 9p21.1 28550930 28582398 31468 loss external link Gai, 2011
AutCNV0003304 9 9p21.1 28529410 28793773 264363 loss external link Gai, 2011
AutCNV0004687 9 9p21.1 28464218 28596286 132068 loss external link Gazzellone MJ, 2014
AutCNV0004686 9 9p21.1 28491679 28630598 138919 loss external link Gazzellone MJ, 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
9 28359590 A T Sanger and Sequenom Michaelson JJ, 2012
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
AutLD0000078 9p21.2-21.3 9 D9S171/D9S161 2.12 - - Lamb, 2005




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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