AutismKB 2.0

Detail Information of AutCNV0005012

1. Sample AND Method Top
Users can click the chromosome coordinates of "Region" label to view information in UCSC Genome Browser.
Ancestry ADI-R ADOS Diagnosis Family Individual Reference
Total Simplex Multiplex Control Affected Control Total
---- 1 1 - - 1 - 1 Fieremans N, 2015
Complication: Y
Population: -
Platform: -
Method: X chromosome-specific aCGH
Marker:-
Band:Xp11.22
Evidences:CNVs Only Present In Patients; Denovo CNVs;
Region: ChrX: 52920728-53321125
Gain/Loss:loss
2. Related Syndromic Genes Top
Abbreviations: AD, autosomal dominant; AR, autosomal recessive; ASD, autism spectrum disorder; ID, intellectual disability; XL, X linked.
Gene ID Gene Symbol Inheritance Evidence Level
AutG8242 KDM5C XL Level 1: The gene has only been reported in single cases with ASD/autistic features. Additional evidences are needed.
AutG23096 IQSEC2 XL Level 3: The gene has been reported in many families with ASD/autistic features, but the disorder hasn't been a generally acknowledged ASD related disorder.
3. Related Non-syndromic Genes Top
Gene ID Gene Symbol Evidence Score Total Score
Low-Scale Association GWAS Low-Scale Single Gene Expression CNV Linkage
AutG8242 KDM5C 0 0 1 0 1 0 12

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