AutismKB 2.0

Variant Details for ATAD5


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Basic Information Top
Gene Symbol:ATAD5 ( C17orf41,ELG1,FLJ12735,FRAG1 )
Gene Full Name: ATPase family, AAA domain containing 5
Band: 17q11.2
Quick LinksEntrez ID:79915; OMIM: 609534; Uniprot ID:ATAD5_HUMAN; ENSEMBL ID: ENSG00000176208; HGNC ID: 25752
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 2 1 0 0 0 6 9
CNVs/SVs Top
CNV ID Chr Band Start End Size Gain/Loss UCSC Browser Reference
AutCNV0002932 17 17q11.2 29015932 29189903 173971 gain external link Pinto, 2010
AutCNV0005648 17 17 Krumm N, 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
17 29167645 C G PCR or Sanger sequencingneutral0.2415 Iossifov I, 2014
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
AutLD0000039 17q11.2 17 HTTINT2 2.34 - - Monaco, 2001
AutLD0000016 17q11.2 17 D17S1800 2.83 - - Yonan, 2003
AutLD0000008 17q11.2 17 D17S1294 2.85 - - McCauley, 2005
AutLD0000148 17q11.2 17 D17S1800 5.82 4.88 0.000000159 Sutcliffe, 2005
AutLD0000118 17q11.2 17 - - 2.1 - Spence, 2006
AutLD0000108 17q11.2 17 D17S1294 - 2.39 - Ylisaukko-oja, 2006




Simple Query:


  (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