AutismKB 2.0

Variant Details for COPS2


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Basic Information Top
Gene Symbol:COPS2 ( ALIEN,CSN2,SGN2,TRIP15 )
Gene Full Name: COP9 constitutive photomorphogenic homolog subunit 2 (Arabidopsis)
Band: 15q21.2
Quick LinksEntrez ID:9318; OMIM: 604508; Uniprot ID:CSN2_HUMAN; ENSEMBL ID: ENSG00000166200; HGNC ID: 30747
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 1 5 0 0 0 2 8
CNVs/SVs Top
CNV ID Chr Band Start End Size Gain/Loss UCSC Browser Reference
AutCNV0000368 15 15q21.1 44912708 49812708 4900000 external link Zwaag, 2009
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
15 49426143 G A c.899C>T p.Pro300Leu Sanger sequencing deleterious0.998 Jiang YH, 2013
15 49429353 C T Sanger sequencing De Rubeis S, 2014
15 49426143 G A Sanger sequencing deleterious0.998 Yuen RK, 2016
15 49429353 C T Fromer M, 2014
15 49426143 c.C899T deleterious0.998 Jiang YH, 2013
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
AutLD0000156 15q14-q21.1 15 rs723049 3.59 - - Allen-Brady, 2010
AutLD0000158 15q21.1-q22.2 15 rs383902 1.49 - - Allen-Brady, 2010




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  (e.g. CHD8)

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