AutismKB 2.0

Variant Details for GTF2I


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Basic Information Top
Gene Symbol:GTF2I ( BAP135,BTKAP1,DIWS,FLJ38776,FLJ56355,GTFII-I,IB291,SPIN,TFII-I,WBS,WBSCR6 )
Gene Full Name: general transcription factor IIi
Band: 7q11.23
Quick LinksEntrez ID:2969; OMIM: 601679; Uniprot ID:GTF2I_HUMAN; ENSEMBL ID: ENSG00000077809; HGNC ID: 4659
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 9 0 0 0 1 0 10
CNVs/SVs Top
CNV ID Chr Band Start End Size Gain/Loss UCSC Browser Reference
AutCNV0000132 7 7q11 72185990 76985990 4800000 loss external link Jacquemont, 2006
AutCNV0000257 7 7q11.23 73277476 74378974 1101498 gain external link Depienne, 2007
AutCNV0003814 7 7q11.23 72719808 74143620 1423812 gain external link Levy, 2011
AutCNV0004264 7 7q11.23 72773570 74173250 1399680 gain external link Sanders, 2011
AutCNV0004263 7 7q11.23 72717647 74144177 1426530 gain external link Sanders, 2011
AutCNV0004262 7 7q11.23 72706490 74144177 1437687 gain external link Sanders, 2011
AutCNV0004261 7 7q11.23 72662415 74144177 1481762 gain external link Sanders, 2011
AutCNV0003815 7 7q11.23 72739232 74142229 1402997 gain external link Levy, 2011
AutCNV0004978 7 7q11.23 74455447 74488775 33328 external link Sanders SJ, 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
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
Sakurai, 2010
Linkage Regions Top
Linkage Name Band Chr Marker LOD NPL P Value Reference
No related data!




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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