AutismKB 2.0

Variant Details for AGRN


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Basic Information Top
Gene Symbol:AGRN ( FLJ45064 )
Gene Full Name: agrin
Band: 1p36.33
Quick LinksEntrez ID:375790; OMIM: 103320; Uniprot ID:AGRIN_HUMAN; ENSEMBL ID: ENSG00000188157; HGNC ID: 329
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 3 0 0 0 0 9
CNVs/SVs Top
CNV ID Chr Band Start End Size Gain/Loss UCSC Browser Reference
AutCNV0000441 1 1p36.32-36.33 10001 3706053 3696052 loss external link Gregory, 2009
AutCNV0000347 1 1p36.33 Zwaag, 2009
AutCNV0000346 1 1p36.33 Zwaag, 2009
AutCNV0000442 1 1p36.32-36.33 869049 3706053 2837004 gain external link Gregory, 2009
AutCNV0000976 1 1p36.33 838555 989461 150906 gain external link Pinto, 2010
AutCNV0003119 1 1p36.32-36.33 10002 5170712 5160710 loss external link Gai, 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
1 981205 T C Sanger sequencing deleterious0.9994 Yuen RK, 2016
1 955717 C T c.165C>T p.Leu55Leu Not_tested Takata A, 2018
1 980641 CCTGGCTGG C c.2359_2366delGCTGGCTG p.Ala787fs Sanger sequencing Takata A, 2018
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