AutismKB 2.0

Annotation Details for ERCC6L


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Basic Information Top
Gene Symbol:ERCC6L ( FLJ20105,MGC131695,PICH )
Gene Full Name: excision repair cross-complementing rodent repair deficiency, complementation group 6-like
Band: Xq13.1
Quick LinksEntrez ID:54821; OMIM: 300687; Uniprot ID:ERC6L_HUMAN; ENSEMBL ID: ENSG00000186871; HGNC ID: 20794
Relate to Another Database: SFARIGene; denovo-db
Gene Ontology Top
GO ID Evidence Qualifier GO_term References
GO:0000777IEA-condensed chromosome kinetochore-
GO:0005829TAS-cytosol-
GO:0016020IDA-membrane19946888
GO ID Evidence Qualifier GO_term References
GO:0003677IEA-DNA binding-
GO:0004386IEA-helicase activity-
GO:0005515IPI-protein binding20360068
GO:0005524IEA-ATP binding-
GO ID Evidence Qualifier GO_term References
GO:0007062TAS-sister chromatid cohesion-
GO:0051301IEA-cell division-
Protein-Protein Interaction Top
Gene Symbol Interactant Interaction ID References Description
ERCC6LPLK112017619596235 Affinity Capture-MS
ERCC6LPLK111136219596235 Affinity Capture-MS
ERCC6LRPA312017617353931 Affinity Capture-MS
ERCC6LRPA311203917353931 Affinity Capture-MS
ERCC6LRB1CC112017617353931 Affinity Capture-MS
ERCC6LRB1CC111516017353931 Affinity Capture-MS
No data
No data
AlzGene, PDGene and SZGene Top
Animal Model Top
  • MGI ID: MGI:2654144
  • 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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