AutismKB 2.0

Annotation Detail for OLIG3


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Basic Information Top
Gene Symbol:OLIG3 ( Bhlhb7,bHLHe20 )
Gene Full Name: oligodendrocyte transcription factor 3
Band: 6q23.3
Quick LinksEntrez ID:167826; OMIM: 609323; Uniprot ID:OLIG3_HUMAN; ENSEMBL ID: ENSG00000177468; HGNC ID: 18003
Relate to Another Database: SFARIGene; denovo-db
Post Translation Modification Top
No data
No data
Location(AA) Modification Resource
7Phosphoserine(CK1)HMM predict
13Phosphoserine(IKK)HMM predict
14Phosphoserine(CAMK2)HMM predict
39Phosphoserine(IKK)HMM predict
140Phosphoserine(IKK)HMM predict
167O-linkedHMM predict
193N-linkedHMM predict
196Phosphoserine(CDC2)HMM predict
208Phosphothreonine(PKC)HMM predict
221Phosphothreonine(MAPK)HMM predict
221Phosphothreonine(CDK)HMM predict
239S-palmitoylHMM predict
Validated transcription factor binding site by ChIP-Chip and ChIP-Seq
  • RefSeq ID: NM_175747
  • Location:chr6 137855028-137857223
  • strand:-
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF G2GSE9613 137860485 137861114 629 3576
H3K27me3 colorectalcancer 137856444 137860134 3690 1066
H3K27me3 colorectalcancer 137860944 137862253 1309 4375
NRSF-poly JurkatQuESTdata 137875467 137875982 515 18501
hScc1 BcellGSE12603 137858040 137858426 386 1010
hScc1 BcellGSE12603 137860656 137861081 425 3645
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF G2GSE9613 137850535 137851333 798 4095
CTCF G2GSE9613 137851569 137851821 252 3334
Oct1 HelaGSE14283 137849390 137849449 59 5609
Oct1 HelaGSE14283 137850839 137850873 34 4173
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF G2GSE9613 137855930 137856412 482 0
H3K27me3 colorectalcancer 137854794 137856078 1284 0
hScc1 BcellGSE12603 137855966 137856373 407 0
Validated miRNA targets Top
Cis-Nats regulation 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