AutismKB 2.0

Annotation Detail for WDR86


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Basic Information Top
Gene Symbol:WDR86 ( FLJ51355,MGC129839 )
Gene Full Name: WD repeat domain 86
Band: 7q36.1
Quick LinksEntrez ID:349136; OMIM: NA; Uniprot ID:WDR86_HUMAN; ENSEMBL ID: ENSG00000187260; HGNC ID: 28020
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_198285
  • Location:chr7 150709146-150738672
  • strand:-
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
H3K27me3 colorectalcancer 150738720 150740658 1938 1017
No data
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF CD4GSE12889 150736782 150737006 224 0
CTCF CD4SISSRdata 150736782 150737006 224 0
CTCF G2GSE9613 150709511 150709762 251 0
CTCF G2GSE9613 150713933 150715796 1863 0
CTCF G2GSE9613 150718072 150718483 411 0
CTCF G2GSE9613 150721060 150721499 439 0
CTCF G2GSE9613 150723108 150723300 192 0
CTCF G2GSE9613 150723711 150724200 489 0
CTCF G2GSE9613 150725856 150726074 218 0
CTCF G2GSE9613 150728063 150728210 147 0
CTCF G2GSE9613 150730432 150730781 349 0
CTCF G2GSE9613 150737495 150737961 466 0
Gata2 K562GSE18868 150723192 150723936 744 0
NRSF pAbJurkat 150730432 150730640 208 0
P300 T0-glioblastomaGSE21026 150731085 150732166 1081 0
RARA MCF7GSE15244 150731800 150733036 1236 0
TFAP2C MCF7GSE21234 150723103 150723422 319 0
hScc1 BcellGSE12603 150723108 150723300 192 0
hScc1 BcellGSE12603 150737757 150738133 376 0
hScc1 G2GSE9613 150713784 150714782 998 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
24869 EST chr7 150545295 150546741 62 mRNA LOC349136 chr7 150515861 150545388Sense/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