AutismKB 2.0

Annotation Details for SNX22


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Basic Information Top
Gene Symbol:SNX22 ( FLJ13952 )
Gene Full Name: sorting nexin 22
Band: 15q22.31
Quick LinksEntrez ID:79856; OMIM: NA; Uniprot ID:SNX22_HUMAN; ENSEMBL ID: ENSG00000157734; HGNC ID: 16315
Relate to Another Database: SFARIGene; denovo-db
Gene Ontology Top
GO ID Evidence Qualifier GO_term References
GO:0030659IEA-cytoplasmic vesicle membrane-
GO ID Evidence Qualifier GO_term References
GO:0035091IEA-phosphatidylinositol binding-
GO ID Evidence Qualifier GO_term References
GO:0015031IEA-protein transport-
Protein-Protein Interaction Top
Gene Symbol Interactant Interaction ID References Description
SNX22DVL312294516189514 Two-hybrid
SNX22DVL310819016189514 Two-hybrid
No data
No data
AlzGene, PDGene and SZGene Top
Animal Model Top
  • MGI ID: MGI:2685966
  • Data Attributes: MGI curated and HomoloGene calculated
No data
No data

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


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