AutismKB 2.0

Annotation Detail for ZNF215


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Basic Information Top
Gene Symbol:ZNF215 ( BAZ-2,BAZ2,ZKSCAN11 )
Gene Full Name: zinc finger protein 215
Band: 11p15.4
Quick LinksEntrez ID:7762; OMIM: 605016; Uniprot ID:ZN215_HUMAN; ENSEMBL ID: ENSG00000149054; HGNC ID: 13007
Relate to Another Database: SFARIGene; denovo-db
Post Translation Modification Top
No data
No data
Location(AA) Modification Resource
56Phosphotyrosine(Jak)HMM predict
67Phosphoserine(ATM)HMM predict
67Phosphoserine(CK1)HMM predict
174Phosphoserine(CK1)HMM predict
295SulfotyrosineHMM predict
295Phosphotyrosine(SRC)HMM predict
357SulfotyrosineHMM predict
421N-linkedHMM predict
450Phosphoserine(IKK)HMM predict
452N-linkedHMM predict
462Phosphotyrosine(EGFR)HMM predict
472N-linkedHMM predict
476Phosphoserine(CK1)HMM predict
495S-palmitoylHMM predict
513Phosphothreonine(PKC)HMM predict
Validated transcription factor binding site by ChIP-Chip and ChIP-Seq
  • RefSeq ID: NM_013250
  • Location:chr11 6904229-6935852
  • strand:+
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
GABP k562GSE8489 6903360 6904326 966 387
No data
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
H3K4me2 HCT116GSE10453 6905077 6905722 645 0
H3K4me3 colorectalcancer 6903895 6904785 890 0
H3K4me3 colorectalcancer 6905223 6905549 326 0
hScc1 CdLSGSE12603 6903996 6904698 702 0
p130 QuiescentGSE19898 6904132 6904794 662 0
p130 SenescentGSE19898 6904223 6904889 666 0
p130 shRbQuiescentGSE19898 6904068 6904763 695 0
p130 shRbSenescentGSE19898 6904122 6904918 796 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
4077 mRNA ZNF215 chr11 6904229 6935644 263 EST chr11 6875957 6904674Sense/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


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