Evidence Detail for TSNAX

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Basic Information Top
Gene Symbol:TSNAX ( DISC1,TRAX )
Gene Full Name: translin-associated factor X
Band: 1q42.1
Quick LinksEntrez ID:7257; OMIM: 602964; Uniprot ID:TSNAX_HUMAN; ENSEMBL ID: ENSG00000116918
Sequences Top
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Evidence Statistic Top

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Evidences Syndromic Gene GWAS Expression CNV Linkage Low Scale Association Other Studies Total
Score (No. of Studies) No 0 (0) 0 (0) 0 (0) 0 (0) 0 (0) 1 (1) 7 (1)
Syndromic Autism Gene Top
Low Scale Association Studies (by Ethnic Group) Top
Genome-Wide Association Studies(By Ethnic Group) Top
Other Low Scale Gene Studies Top
Reference Orangnism Tissue ADI-R ADOS Diagnosis Evidence Level Result
Williams, 2009_3 human bloodASD case report
  • Subjects: a 3-year-old male with no family history
  • Normal Controls: -
  • Methods: array comparative genome hybridization (aCGH) analysis
  • Evidence Details: Here we report a 3-year-old male with developmental delay and autistic behaviors who has an interstitial of deletion 1q42. The deletion spans approximately 2?Mb, involves DISC1, DISC2, and TSNAX and was inherited from his nonaffected mother.
Large Scale Expression Studies Top
CNV Studies Top
Linkage Studies Top

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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
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