AutismKB 2.0

Annotation Detail for SCO2


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Basic Information Top
Gene Symbol:SCO2 ( MGC125823,MGC125825,SCO1L )
Gene Full Name: SCO cytochrome oxidase deficient homolog 2 (yeast)
Band: 22q13.33
Quick LinksEntrez ID:9997; OMIM: 604272; Uniprot ID:SCO2_HUMAN; ENSEMBL ID: ENSG00000130489; HGNC ID: 10604
Relate to Another Database: SFARIGene; denovo-db
Post Translation Modification Top
Validated transcription factor binding site by ChIP-Chip and ChIP-Seq
  • RefSeq ID: NM_005138
  • Location:chr22 49308864-49310837
  • strand:-
No data
No data
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF G2GSE9613 49309502 49309861 359 0
H3ac HepG2E 49309760 49310557 797 0
PHF8 HeLaGSE20725 49309089 49312581 3492 0
USF1 HepG2E 49309826 49310593 767 0
hScc1 BcellGSE12603 49308413 49312133 3720 0
Validated miRNA targets Top
Cis-Nats regulation Top
Cluster ID Plue Type Plus Gene Name Plus Chromosome Plus Start Plus End Overlap Length Minus Type Minus Gene Name Minus Chromosome Minus Star Minus End Type
17671 EST chr22 49251107 49252309 157 mRNA SCO2 chr22 49252142 49254116Sense/Antisense (SA) pairs

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