AutismKB

Detail Information of AutCNV0004851

1. Sample AND Method Top
Ancestry ADI-R ADOS Diagnosis Family Individual Reference
Total Simplex Multiplex Control Affected Control Total
Caucasionautism, ASD 912 - 912 - - 1488 - Bucan, 2009
Population: USA
Platform: Illumina HumanHap550 version 3 array
Method: SNP microarray
Marker:edels
Band:2p16.3
Evidences:Overlapping/Recurrent CNVs; CNVs Not Present In Control;
Region: Chr2: 50000992 - 51113178
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
AutG9378 NRXN1 AD?/AR (Pitt-Hopkins-like) 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
AutG9378 NRXN1 1 0 3 0 2 0 28

Quick Search:


  (e.g. NLGN4X)

Syndromic Genes

Non-syndromic Genes

AutismKB Statistics

  • Studies: 616
  • Genes: 3,075
  • SNPs/VNTRs: 3,386
  • CNVs: 4,617
  • Linkage Regions: 158
  • Last Update: 05/25/2012
  • Click to Download Data

Registered with NIF