AutismKB 2.0

Annotation Detail for CKAP5


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Basic Information Top
Gene Symbol:CKAP5 ( CHTOG,FLJ35359,KIAA0097,MSPS,TOG,TOGp,ch-TOG )
Gene Full Name: cytoskeleton associated protein 5
Band: 11p11.2
Quick LinksEntrez ID:9793; OMIM: 611142; Uniprot ID:CKAP5_HUMAN; ENSEMBL ID: ENSG00000175216; HGNC ID: 28959
Relate to Another Database: SFARIGene; denovo-db
Post Translation Modification Top
Location(AA) Modification
48N6-acetyllysine.
816Phosphoserine.
Location(AA) Modifications Resource
816Phosphoserine.Swiss-Prot 53.0
816PhosphoserinePhospho.ELM 6.0
Location(AA) Modification Resource
26Phosphoserine(PKG)HMM predict
28Phosphotyrosine(EGFR)HMM predict
223O-linkedHMM predict
285Phosphotyrosine(Syk)HMM predict
317Phosphotyrosine(INSR)HMM predict
392O-linkedHMM predict
409N-linkedHMM predict
449N-linkedHMM predict
673N-linkedHMM predict
725Phosphoserine(ATM)HMM predict
731N-linkedHMM predict
737N-linkedHMM predict
767O-linkedHMM predict
816Phosphoserine(ATM)HMM predict
816Phosphoserine(IKK)HMM predict
828Phosphoserine(IKK)HMM predict
862Phosphothreonine(CK2)HMM predict
1008Phosphothreonine(PKC)HMM predict
1115Phosphoserine(CK1)HMM predict
1184N-linkedHMM predict
1187Phosphothreonine(CDC2)HMM predict
1192SulfotyrosineHMM predict
1280Phosphotyrosine(SRC)HMM predict
1428PhosphoserineHMM predict
1461Phosphoserine(CK1)HMM predict
1462Phosphoserine(CK1)HMM predict
1471Phosphoserine(PKB)HMM predict
1495N-linkedHMM predict
1702Phosphoserine(CDC2)HMM predict
1846Phosphothreonine(CK2)HMM predict
1858MethyllysineHMM predict
1859MethyllysineHMM predict
1861Phosphoserine(CK2)HMM predict
1871N-linkedHMM predict
1898Phosphoserine(PKG)HMM predict
1914Phosphothreonine(CDK)HMM predict
1914Phosphothreonine(MAPK)HMM predict
1914O-linkedHMM predict
1914O-linkedHMM predict
1916O-linkedHMM predict
1917Phosphoserine(IKK)HMM predict
1918O-linkedHMM predict
1920O-linkedHMM predict
1970Phosphothreonine(PKC)HMM predict
2000N-linkedHMM predict
2007O-linkedHMM predict
2009O-linkedHMM predict
2010O-linkedHMM predict
2011O-linkedHMM predict
2027IsoleucineHMM predict
Validated transcription factor binding site by ChIP-Chip and ChIP-Seq
  • RefSeq ID: NM_001008938
  • Location:chr11 46721659-46824418
  • strand:-
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
E2F4 G0GSE7516 46824202 46824743 541 54
H3ac HepG2E 46825082 46825379 297 812
LIN9 SGSE7516 46824202 46824743 541 54
LIN9 SGSE7516 46825082 46825379 297 812
Myc hESGSE17917 46824246 46824619 373 14
Nanog ESGSE20650 46828899 46829500 601 4781
Oct4 hESGSE17917 46824340 46824612 272 58
P300 T0-glioblastomaGSE21026 46824146 46824994 848 152
p130 QuiescentGSE19898 46824270 46824634 364 34
p130 SenescentGSE19898 46824202 46824915 713 140
p130 G0GSE7516 46824202 46824743 541 54
p130 SGSE7516 46824238 46824743 505 72
No data
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF CD4GSE12889 46787030 46787177 147 0
CTCF CD4SISSRdata 46787030 46787177 147 0
FOXA1 MCF7GSE15244 46804294 46805320 1026 0
Fos K562GSE19551 46823941 46824824 883 0
FoxA1 MCF7MACSdata 46787068 46787276 208 0
H3ac HepG2E 46823178 46823675 497 0
LIN9 G0GSE7516 46824012 46824743 731 0
Myc K562GSE19551 46799912 46800082 170 0
Nanog ESGSE20650 46743836 46744323 487 0
Nanog hESGSE18292 46743965 46744349 384 0
Oct1 H2O2-HelaGSE14283 46788061 46788100 39 0
Oct1 HelaGSE14283 46780451 46780478 27 0
Oct1 HelaGSE14283 46788060 46788099 39 0
P300 T30-glioblastomaGSE21026 46823647 46825061 1414 0
PHF8 293TGSE20725 46823496 46824763 1267 0
PHF8 HeLaGSE20725 46823465 46824811 1346 0
RARA MCF7GSE15244 46803991 46805492 1501 0
RARG MCF7GSE15244 46804294 46805428 1134 0
TAF HelaGSE8489 46739607 46739785 178 0
TAF HelaGSE8489 46823178 46823779 601 0
TAF k562GSE8489 46823139 46823675 536 0
TFAP2C MCF7GSE21234 46811057 46811387 330 0
hScc1 BcellGSE12603 46823848 46824238 390 0
p130 shRbQuiescentGSE19898 46823923 46824723 800 0
p130 shRbSenescentGSE19898 46823673 46824775 1102 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


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