AutismKB 2.0

Annotation Details for CCDC22


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Basic Information Top
Gene Symbol:CCDC22 ( CXorf37 )
Gene Full Name: coiled-coil domain containing 22
Band: Xp11.23
Quick LinksEntrez ID:28952; OMIM: NA; Uniprot ID:CCD22_HUMAN; ENSEMBL ID: ENSG00000101997; HGNC ID: 28909
Relate to Another Database: SFARIGene; denovo-db
Gene Ontology Top
GO ID Evidence Qualifier GO_term References
GO:0005575ND-cellular_component-
GO:0005654TAS-nucleoplasm-
GO:0005768IEA-endosome-
GO:0005829TAS-cytosol-
GO ID Evidence Qualifier GO_term References
GO:0005515IPI-protein binding23563313
GO:0097602IDA-cullin family protein binding23563313
GO ID Evidence Qualifier GO_term References
GO:0006878IMP-cellular copper ion homeostasis25355947
GO:0006893IMP-Golgi to plasma membrane transport25355947
GO:0007253IMP-cytoplasmic sequestering of NF-kappaB23563313
GO:0015031IEA-protein transport-
GO:0016567TAS-protein ubiquitination-
GO:0043123IMP-positive regulation of I-kappaB kinase/NF-kappaB signaling23563313
GO:0043124IMP-negative regulation of I-kappaB kinase/NF-kappaB signaling23563313
GO:0043687TAS-post-translational protein modification-
GO:2000060IMP-positive regulation of protein ubiquitination involved in ubiquitin-dependent protein catabolic process23563313
Protein-Protein Interaction Top
AlzGene, PDGene and SZGene Top
Animal Model Top
  • MGI ID: MGI:1859608
  • 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