AutismKB 2.0

Annotation Details for C22orf29


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Basic Information Top
Gene Symbol:C22orf29 ( FLJ21125 )
Gene Full Name: chromosome 22 open reading frame 29
Band: 22q11.21
Quick LinksEntrez ID:79680; OMIM: NA; Uniprot ID:CV029_HUMAN; ENSEMBL ID: ENSG00000215012; HGNC ID:
Relate to Another Database: SFARIGene; denovo-db
Gene Ontology Top
GO ID Evidence Qualifier GO_term References
GO:0005739IDA-mitochondrion23055042
GO ID Evidence Qualifier GO_term References
GO:0005515IPI-protein binding23055042
GO ID Evidence Qualifier GO_term References
GO:0051881IMP-regulation of mitochondrial membrane potential23055042
GO:0097345IMP-mitochondrial outer membrane permeabilization23055042
Protein-Protein Interaction Top
AlzGene, PDGene and SZGene Top
Animal Model 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