AutismKB 2.0

Variant Details for OPCML


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Basic Information Top
Gene Symbol:OPCML ( IGLON1,OBCAM,OPCM )
Gene Full Name: opioid binding protein/cell adhesion molecule-like
Band: 11q25
Quick LinksEntrez ID:4978; OMIM: 600632; Uniprot ID:OPCM_HUMAN; ENSEMBL ID: ENSG00000183715; HGNC ID: 8143
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 7 1 0 0 0 0 8
CNVs/SVs Top
CNV ID Chr Band Start End Size Gain/Loss UCSC Browser Reference
AutCNV0000093 11 11q23.2-25 113996790 134897790 20901000 gain external link Szatmari, 2007
AutCNV0000362 11 11q25 130794790 134946516 4151726 external link Zwaag, 2009
AutCNV0002015 11 11q25 132882164 132932983 50819 gain external link Pinto, 2010
AutCNV0003337 11 11q25 133110021 133336402 226381 gain external link Gai, 2011
AutCNV0003336 11 11q25 133093579 133336562 242983 gain external link Gai, 2011
AutCNV0004297 11 11q24.2-q25 127128729 132555164 5426435 loss external link Sanders, 2011
AutCNV0005098 8 8q22.2q22.3 100142380 103492901 3350521 loss external link Sinajon P, 2015
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
11 133255038 C 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
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