AutismKB 2.0

Annotation Detail for SIAH3


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Basic Information Top
Gene Symbol:SIAH3 ( FLJ39203 )
Gene Full Name: seven in absentia homolog 3 (Drosophila)
Band: 13q14.13
Quick LinksEntrez ID:283514; OMIM: NA; Uniprot ID:SIAH3_HUMAN; ENSEMBL ID: ENSG00000215475; HGNC ID: 30553
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_198849
  • Location:chr13 45252417-45323846
  • strand:-
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF G2GSE9613 45336910 45337079 169 13148
ER Fulvestrant-MCF7GSE14664 45337365 45337397 32 13535
Oct1 HelaGSE14283 45337363 45337400 37 13535
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
Oct1 H2O2-HelaGSE14283 45232713 45232743 30 19690
Oct1 HelaGSE14283 45232712 45232746 34 19689
Oct1 HelaGSE14283 45241397 45241428 31 11005
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF G2GSE9613 45255716 45256388 672 0
CTCF G2GSE9613 45256690 45256881 191 0
CTCF G2GSE9613 45291471 45291839 368 0
CTCF G2GSE9613 45320050 45320331 281 0
CTCF G2GSE9613 45322746 45323103 357 0
H3K27me3 colorectalcancer 45322006 45324155 2149 0
Jun K562GSE19551 45279677 45280056 379 0
Nanog hESGSE18292 45289977 45290299 322 0
Oct1 H2O2-HelaGSE14283 45298862 45298895 33 0
Oct1 HelaGSE14283 45268127 45268162 35 0
Oct1 HelaGSE14283 45298862 45298895 33 0
Oct1 HelaGSE14283 45307392 45307422 30 0
RARG MCF7GSE15244 45323029 45324115 1086 0
TFAP2C MCF7GSE21234 45284009 45284597 588 0
VDR GM10855-stimGSE22484 45319215 45320226 1011 0
VDR GM10861-stimGSE22484 45319189 45320418 1229 0
hScc1 BcellGSE12603 45279661 45279910 249 0
hScc1 CdLSGSE12603 45279636 45279910 274 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