AutismKB 2.0

Annotation Detail for STAP2


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Basic Information Top
Gene Symbol:STAP2 ( BKS,FLJ20234 )
Gene Full Name: signal transducing adaptor family member 2
Band: 19p13.3
Quick LinksEntrez ID:55620; OMIM: 607881; Uniprot ID:STAP2_HUMAN; ENSEMBL ID: ENSG00000178078; HGNC ID: 30430
Relate to Another Database: SFARIGene; denovo-db
Post Translation Modification Top
Location(AA) Modification
22Phosphotyrosine; by SRC (Probable).
250Phosphotyrosine (Probable).
310Phosphotyrosine (Probable).
322Phosphotyrosine; by SRC (Probable).
Location(AA) Modifications Resource
22Phosphotyrosine (by SRC) (Probable).Swiss-Prot 53.0
250Phosphotyrosine (Probable).Swiss-Prot 53.0
310Phosphotyrosine (Probable).Swiss-Prot 53.0
322Phosphotyrosine (by SRC) (Probable).Swiss-Prot 53.0
Location(AA) Modification Resource
22Phosphotyrosine(Syk)HMM predict
102Phosphothreonine(PKC)HMM predict
150Phosphothreonine(MAPK)HMM predict
196N-linkedHMM predict
250Phosphotyrosine(Syk)HMM predict
250Phosphotyrosine(Jak)HMM predict
272O-linkedHMM predict
289Phosphoserine(CDC2)HMM predict
289Phosphoserine(IKK)HMM predict
289Phosphoserine(MAPK)HMM predict
293Phosphoserine(ATM)HMM predict
310Phosphotyrosine(INSR)HMM predict
310Phosphotyrosine(Abl)HMM predict
310Phosphotyrosine(EGFR)HMM predict
329Phosphoserine(CK1)HMM predict
373O-linkedHMM predict
Validated transcription factor binding site by ChIP-Chip and ChIP-Seq
  • RefSeq ID: NM_001013841
  • Location:chr19 4275040-4289846
  • strand:-
No data
No data
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
ER E2-MCF7GSE14664 4280425 4280457 32 0
H3ac HepG2E 4289227 4289878 651 0
Oct1 HelaGSE14283 4279166 4279224 58 0
Oct1 HelaGSE14283 4280071 4280116 45 0
TFAP2C MCF7GSE21234 4289605 4289967 362 0
hScc1 BcellGSE12603 4278285 4278918 633 0
hScc1 BcellGSE12603 4279657 4279952 295 0
hScc1 BcellGSE12603 4280401 4280945 544 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