AutismKB 2.0

Annotation Details for SNX19


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Basic Information Top
Gene Symbol:SNX19 ( CHET8,DKFZp667I205,KIAA0254 )
Gene Full Name: sorting nexin 19
Band: 11q24.3-q25
Quick LinksEntrez ID:399979; OMIM: NA; Uniprot ID:SNX19_HUMAN; ENSEMBL ID: ENSG00000120451; HGNC ID: 21532
Relate to Another Database: SFARIGene; denovo-db
Gene Ontology Top
GO ID Evidence Qualifier GO_term References
GO:0005737IDA-cytoplasm19877062
GO:0030659IEA-cytoplasmic vesicle membrane-
GO:0031901IEA-early endosome membrane-
GO ID Evidence Qualifier GO_term References
GO:0005515IPI-protein binding16273344
GO:0032266IEA-phosphatidylinositol-3-phosphate binding-
GO ID Evidence Qualifier GO_term References
GO:0002062IMP-chondrocyte differentiation19877062
GO:0006887IEA-exocytosis-
GO:0030073IGI-insulin secretion24843546
GO:1990502IGI-dense core granule maturation24843546
Protein-Protein Interaction Top
AlzGene, PDGene and SZGene Top
Animal Model Top
  • MGI ID: MGI:1921581
  • 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