AutismKB 2.0

Annotation Details for C19orf26


View Evidences View Variants View Annotations
Basic Information Top
Gene Symbol:C19orf26 ( DOS,MGC40084 )
Gene Full Name: chromosome 19 open reading frame 26
Band: 19p13.3
Quick LinksEntrez ID:255057; OMIM: NA; Uniprot ID:DOS_HUMAN; ENSEMBL ID: ENSG00000099625; HGNC ID:
Relate to Another Database: SFARIGene; denovo-db
Gene Ontology Top
GO ID Evidence Qualifier GO_term References
GO:0005886ISS-plasma membrane-
GO:0016021IEA-integral component of membrane-
GO:0030054IEA-cell junction-
GO:0030141ISS-secretory granule-
GO:0030426ISScolocalizes_withgrowth cone-
GO:0030672IEA-synaptic vesicle membrane-
GO ID Evidence Qualifier GO_term References
GO:0044325ISS-ion channel binding-
GO ID Evidence Qualifier GO_term References
GO:0045955ISS-negative regulation of calcium ion-dependent exocytosis-
GO:1901386ISS-negative regulation of voltage-gated calcium channel activity-
GO:1903170ISS-negative regulation of calcium ion transmembrane transport-
Protein-Protein Interaction Top
AlzGene, PDGene and SZGene Top
Animal Model Top
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