AutismKB 2.0

Annotation Detail for C20orf132


View Evidences View Variants View Annotations
Basic Information Top
Gene Symbol:C20orf132 ( C20orf131,DKFZp434N0426,FLJ36113,dJ621N11.3,dJ621N11.4 )
Gene Full Name: chromosome 20 open reading frame 132
Band: 20q11.22
Quick LinksEntrez ID:140699; OMIM: NA; Uniprot ID:CT132_HUMAN; ENSEMBL ID: ENSG00000101353; HGNC ID:
Relate to Another Database: SFARIGene; denovo-db
Related Pathway Information Top
Related Diseases/Disorders Top
No data
No data
Desease Name
NEUROLOGICAL
hippocampal atrophy
No data
No data
Comparative Toxicogenomics Database Top
Pharmacogenomics Knowledge Base Top
Drug Bank Top

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